A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042668



Internal ID18785199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23319713..23678449hg38UCSC Ensembl
Innerchr15:23482349..23923596hg19UCSC Ensembl
Innerchr15:21033790..21474689hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38358737
hg19441248
hg18440900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3538884
Samples
Known GenesGOLGA8S, LOC440243, MAGEL2, MIR4508, MKRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042668
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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