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dbVar

Database of genomic structural variation

nsv131005

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:9,865

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: 346 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):59,698,661-59,708,525

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv131005	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	59,698,661	59,708,525
nsv131005	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	57,365,893	57,375,757
nsv131005	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000018.8	Chr18	55,516,873	55,526,737

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv149583	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv149583	Remapped	Perfect	NC_000018.10:g.596 98661_59708525del9 865	GRCh38.p12	First Pass	NC_000018.10	Chr18	59,698,661	59,708,525
nssv149583	Remapped	Perfect	NC_000018.9:g.5736 5893_57375757del98 65	GRCh37.p13	First Pass	NC_000018.9	Chr18	57,365,893	57,375,757
nssv149583	Submitted genomic		NC_000018.8:g.5551 6873_55526737del98 65	NCBI35 (hg17)		NC_000018.8	Chr18	55,516,873	55,526,737

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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