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dbVar

Database of genomic structural variation

nsv290685

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:9,989

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: 317 SVs from 50 studies. See in: genome view

Remapped(Score: Perfect):134,147,772-134,157,760

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv290685	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	134,147,772	134,157,760
nsv290685	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	135,068,927	135,078,915
nsv290685	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000004.9	Chr4	135,426,532	135,436,520

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv309263	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv309263	Remapped	Perfect	NC_000004.12:g.134 147772_134157760de l9989	GRCh38.p12	First Pass	NC_000004.12	Chr4	134,147,772	134,157,760
nssv309263	Remapped	Perfect	NC_000004.11:g.135 068927_135078915de l9989	GRCh37.p13	First Pass	NC_000004.11	Chr4	135,068,927	135,078,915
nssv309263	Submitted genomic		NC_000004.9:g.1354 26532_135436520del 9989	NCBI35 (hg17)		NC_000004.9	Chr4	135,426,532	135,436,520

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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