A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904101



Internal ID6266028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40987725..41257324hg19UCSC Ensembl
Outerchr15:40979651..41275014hg19UCSC Ensembl
Innerchr15:38775017..39044616hg18UCSC Ensembl
Outerchr15:38766943..39062306hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546869
SamplesMS17208
Known GenesC15orf62, CHAC1, DLL4, DNAJC17, FAM82A2, GCHFR, INO80, LOC100505648, PPP1R14D, RAD51, RHOV, SPINT1, VPS18, ZFYVE19
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904101
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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