A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036398



Internal ID19125617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67912019..68032735hg38UCSC Ensembl
Innerchr15:68204357..68325073hg19UCSC Ensembl
Innerchr15:65991411..66112127hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38120717
hg19120717
hg18120717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553653
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)nsv1036398
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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