A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054102



Internal ID18796633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42200854..42236567hg38UCSC Ensembl
Innerchr15:42493052..42528765hg19UCSC Ensembl
Innerchr15:40280344..40316057hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3835714
hg1935714
hg1835714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552277
Samples
Known GenesTMEM87A, VPS39
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054102
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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