A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041242



Internal ID19130461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85796276..85807277hg38UCSC Ensembl
Innerchr15:86339507..86350508hg19UCSC Ensembl
Innerchr15:84140511..84151512hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3811002
hg1911002
hg1811002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2652n100
Supporting Variantsnssv3555089
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041242
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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