A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038660



Internal ID19127879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54463986..54747715hg38UCSC Ensembl
Innerchr15:54756184..55039913hg19UCSC Ensembl
Innerchr15:52543476..52827205hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38283730
hg19283730
hg18283730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552435
Samples
Known GenesUNC13C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038660
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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