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dbVar

Database of genomic structural variation

nsv4658787

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:1,045

Description:nsv4579371 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: 128 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):155,020,866-155,021,910

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4658787	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	155,020,866	155,021,910
nsv4658787	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	154,993,342	154,994,386

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16188051	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16188051	Remapped	Perfect	NC_000001.11:g.(?_ 155020866)_(155021 910_?)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,020,866	155,021,910
nssv16188051	Submitted genomic		NC_000001.10:g.(?_ 154993342)_(154994 386_?)del	GRCh37 (hg19)		NC_000001.10	Chr1	154,993,342	154,994,386

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)
nssv16188051	0.055	105	1892

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