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dbVar

Database of genomic structural variation

nsv179259

Organism: Homo sapiens

Study:nstd6 (Mills et al. 2006)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:9,931

Publication(s):Mills et al. 2006

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: 126 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):19,928,157-19,938,087

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv179259	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	19,928,157	19,938,087
nsv179259	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	19,908,801	19,918,731
nsv179259	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000020.9	Chr20	19,856,801	19,866,731

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv197837	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv197837	Remapped	Perfect	NC_000020.11:g.199 28157_19938087del9 931	GRCh38.p12	First Pass	NC_000020.11	Chr20	19,928,157	19,938,087
nssv197837	Remapped	Perfect	NC_000020.10:g.199 08801_19918731del9 931	GRCh37.p13	First Pass	NC_000020.10	Chr20	19,908,801	19,918,731
nssv197837	Submitted genomic		NC_000020.9:g.1985 6801_19866731del99 31	NCBI35 (hg17)		NC_000020.9	Chr20	19,856,801	19,866,731

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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