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dbVar

Database of genomic structural variation

nsv4666099

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:1,204

Description:nsv4620760 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: 114 SVs from 31 studies. See in: genome view

Remapped(Score: Perfect):46,835,803-46,837,006

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4666099	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	46,835,803	46,837,006
nsv4666099	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	47,339,060	47,340,263

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16182597	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16182597	Remapped	Perfect	NC_000019.10:g.(?_ 46835803)_(4683700 6_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	46,835,803	46,837,006
nssv16182597	Submitted genomic		NC_000019.9:g.(?_4 7339060)_(47340263 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	47,339,060	47,340,263

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)
nssv16182597	0.027	12	450

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