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dbVar

Database of genomic structural variation

nsv3068159

Organism: Homo sapiens

Study:nstd90 (dbSNP curated variants)
Variant Type:delins
Method Type:Curated
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,276

Data Source:HUMANGENOME_JCVI

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: 474 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):1,062,879-1,064,154

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3068159	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	1,062,879	1,064,154
nsv3068159	Remapped	Pass	GRCh38.p12	ALT_REF_LOCI_2	Second Pass	NT_187664.1	Chr17\|NT_1 87664.1	101,232	102,328
nsv3068159	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	966,119	967,394

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis
nssv14040783	delins	1104685546563	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14040783	Remapped	Pass	NT_187664.1:g.1012 32_102328delins681	GRCh38.p12	Second Pass	NT_187664.1	Chr17\|NT_1 87664.1	101,232	102,328
nssv14040783	Remapped	Perfect	NC_000017.11:g.106 2879_1064154delins 681	GRCh38.p12	First Pass	NC_000017.11	Chr17	1,062,879	1,064,154
nssv14040783	Submitted genomic		NC_000017.10:g.966 119_967394delins68 1	GRCh37 (hg19)		NC_000017.10	Chr17	966,119	967,394

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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