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dbVar

Database of genomic structural variation

nsv178936

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:9,919

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: 122 SVs from 19 studies. See in: genome view

Remapped(Score: Perfect):18,743,689-18,753,607

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv178936	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	18,743,689	18,753,607
nsv178936	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	18,724,333	18,734,251
nsv178936	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000020.9	Chr20	18,672,333	18,682,251

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv197514	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv197514	Remapped	Perfect	NC_000020.11:g.187 43689_18753607del9 919	GRCh38.p12	First Pass	NC_000020.11	Chr20	18,743,689	18,753,607
nssv197514	Remapped	Perfect	NC_000020.10:g.187 24333_18734251del9 919	GRCh37.p13	First Pass	NC_000020.10	Chr20	18,724,333	18,734,251
nssv197514	Submitted genomic		NC_000020.9:g.1867 2333_18682251del99 19	NCBI35 (hg17)		NC_000020.9	Chr20	18,672,333	18,682,251

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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