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dbVar

Database of genomic structural variation

nsv431277

Organism: Homo sapiens

Study:nstd12 (Marshall et al. 2008)
Variant Type:complex substitution
Method Type:Merging, SNP array
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,082,735

Publication(s):Marshall et al. 2008

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: 13134 SVs from 121 studies. See in: genome view

Remapped(Score: Pass):20,217,334-22,300,068

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv431277	Remapped	Pass	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	20,217,334	22,300,068
nsv431277	Remapped	Pass	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	20,422,587	22,588,019
nsv431277	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000015.8	Chr15	18,682,601	20,089,383

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv563391	complex substitution	59962L	Merging, SNP array	Merging, SNP genotyping analysis	9

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv563391	Remapped	Pass	GRCh38.p12	First Pass	NC_000015.10	Chr15	20,217,334	22,300,068
nssv563391	Remapped	Pass	GRCh37.p13	First Pass	NC_000015.9	Chr15	20,422,587	22,588,019
nssv563391	Submitted genomic		NCBI35 (hg17)		NC_000015.8	Chr15	18,682,601	20,089,383

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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