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dbVar

Database of genomic structural variation

nsv178798

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:9,648

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: 163 SVs from 38 studies. See in: genome view

Remapped(Score: Perfect):16,224,388-16,234,035

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv178798	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	16,224,388	16,234,035
nsv178798	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	16,205,033	16,214,680
nsv178798	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000020.9	Chr20	16,153,033	16,162,680

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv197376	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv197376	Remapped	Perfect	NC_000020.11:g.162 24388_16234035del9 648	GRCh38.p12	First Pass	NC_000020.11	Chr20	16,224,388	16,234,035
nssv197376	Remapped	Perfect	NC_000020.10:g.162 05033_16214680del9 648	GRCh37.p13	First Pass	NC_000020.10	Chr20	16,205,033	16,214,680
nssv197376	Submitted genomic		NC_000020.9:g.1615 3033_16162680del96 48	NCBI35 (hg17)		NC_000020.9	Chr20	16,153,033	16,162,680

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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