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dbVar

Database of genomic structural variation

nsv437079

Organism: Homo sapiens

Study:nstd17 (Conrad et al. 2005)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:NCBI34 (hg16)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:117,424

Publication(s):Conrad et al. 2005

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1123 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):136,732,934-136,850,357

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv437079	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	136,732,934	136,828,157	136,837,578	136,850,357
nsv437079	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	137,745,177	137,840,400	137,849,821	137,862,600
nsv437079	Submitted genomic		NCBI34 (hg16)	Primary Assembly		NC_000008.8	Chr8	137,716,233	137,811,456	137,820,877	137,833,656

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv466960	copy number loss	NA10835	SNP array	SNP genotyping analysis	Heterozygous	13

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv466960	Remapped	Perfect	NC_000008.11:g.(13 6732934_136828157) _(136837578_136850 357)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,732,934	136,828,157	136,837,578	136,850,357
nssv466960	Remapped	Perfect	NC_000008.10:g.(13 7745177_137840400) _(137849821_137862 600)del	GRCh37.p13	First Pass	NC_000008.10	Chr8	137,745,177	137,840,400	137,849,821	137,862,600
nssv466960	Submitted genomic		NC_000008.8:g.(137 716233_137811456)_ (137820877_1378336 56)del	NCBI34 (hg16)		NC_000008.8	Chr8	137,716,233	137,811,456	137,820,877	137,833,656

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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