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dbVar

Database of genomic structural variation

nsv160731

Organism: Homo sapiens

Study:nstd6 (Mills et al. 2006)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:9,808

Publication(s):Mills et al. 2006

Links to Other Resources

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: 194 SVs from 37 studies. See in: genome view

Remapped(Score: Perfect):200,689,038-200,698,845

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv160731	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	200,689,038	200,698,845
nsv160731	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	200,658,166	200,667,973
nsv160731	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000001.8	Chr1	197,389,823	197,399,630

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv179309	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv179309	Remapped	Perfect	NC_000001.11:g.200 689038_200698845de l9808	GRCh38.p12	First Pass	NC_000001.11	Chr1	200,689,038	200,698,845
nssv179309	Remapped	Perfect	NC_000001.10:g.200 658166_200667973de l9808	GRCh37.p13	First Pass	NC_000001.10	Chr1	200,658,166	200,667,973
nssv179309	Submitted genomic		NC_000001.8:g.1973 89823_197399630del 9808	NCBI35 (hg17)		NC_000001.8	Chr1	197,389,823	197,399,630

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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