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dbVar

Database of genomic structural variation

nsv479140

Organism: Homo sapiens

Study:nstd35 (Kidd et al. 2010)
Variant Type:complex substitution
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4

Description:complex allele - no allele length provided
Publication(s):Kidd et al. 2010

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: 210 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):129,745,806-129,745,809

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv479140	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	129,745,806	129,745,809
nsv479140	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	130,758,052	130,758,055
nsv479140	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000008.9	Chr8	130,827,234	130,827,237

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3014700	complex substitution	SAMN00000376	Sequencing	Sequence alignment	9

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3014700	Remapped	Perfect	GRCh38.p12	First Pass	NC_000008.11	Chr8	129,745,806	129,745,809
nssv3014700	Remapped	Perfect	GRCh37.p13	First Pass	NC_000008.10	Chr8	130,758,052	130,758,055
nssv3014700	Submitted genomic		NCBI36 (hg18)		NC_000008.9	Chr8	130,827,234	130,827,237

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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