Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv94522

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:9,898

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: 283 SVs from 54 studies. See in: genome view

Remapped(Score: Perfect):92,763,189-92,773,086

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv94522	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	92,763,189	92,773,086
nsv94522	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	93,306,419	93,316,316
nsv94522	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000015.8	Chr15	91,107,423	91,117,320

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv113100	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv113100	Remapped	Perfect	NC_000015.10:g.927 63189_92773086del9 898	GRCh38.p12	First Pass	NC_000015.10	Chr15	92,763,189	92,773,086
nssv113100	Remapped	Perfect	NC_000015.9:g.9330 6419_93316316del98 98	GRCh37.p13	First Pass	NC_000015.9	Chr15	93,306,419	93,316,316
nssv113100	Submitted genomic		NC_000015.8:g.9110 7423_91117320del98 98	NCBI35 (hg17)		NC_000015.8	Chr15	91,107,423	91,117,320

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

You are here: NCBI