A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037932



Internal ID19127151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85118039..85168070hg38UCSC Ensembl
Innerchr15:85661270..85711301hg19UCSC Ensembl
Innerchr15:83462274..83512305hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3850032
hg1950032
hg1850032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555063
Samples
Known GenesPDE8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037932
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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