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dbVar

Database of genomic structural variation

nsv3068427

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:1,170

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: 427 SVs from 61 studies. See in: genome view

Remapped(Score: Perfect):505,923-507,092

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3068427	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	505,923	507,092
nsv3068427	Remapped	Perfect	GRCh38.p12	PATCHES	Second Pass	NW_017363817.1	Chr17\|NW_0 17363817.1	65,400	66,569
nsv3068427	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	409,163	410,332

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis
nssv14040998	delins	1104685546255	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14040998	Remapped	Perfect	NW_017363817.1:g.6 5400_66569delins26 0	GRCh38.p12	Second Pass	NW_017363817.1	Chr17\|NW_0 17363817.1	65,400	66,569
nssv14040998	Remapped	Perfect	NC_000017.11:g.505 923_507092delins26 0	GRCh38.p12	First Pass	NC_000017.11	Chr17	505,923	507,092
nssv14040998	Submitted genomic		NC_000017.10:g.409 163_410332delins26 0	GRCh37 (hg19)		NC_000017.10	Chr17	409,163	410,332

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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