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dbVar

Database of genomic structural variation

nsv4661168

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:40,755

Description:nsv4593976 from DECIPHER Consensus CNVs. For a full list of variants now included in nstd186, refer to the mapping file provided here.

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: 351 SVs from 66 studies. See in: genome view

Remapped(Score: Perfect):155,210,698-155,251,452

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4661168	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	155,210,698	155,251,452
nsv4661168	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	155,180,489	155,221,243

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16185533	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16185533	Remapped	Perfect	NC_000001.11:g.(?_ 155210698)_(155251 452_?)dup	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,210,698	155,251,452
nssv16185533	Submitted genomic		NC_000001.10:g.(?_ 155180489)_(155221 243_?)dup	GRCh37 (hg19)		NC_000001.10	Chr1	155,180,489	155,221,243

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16185533	0.04	18	450

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