A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039043



Internal ID18781574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85268380..85470404hg38UCSC Ensembl
Innerchr15:85811611..86013635hg19UCSC Ensembl
Innerchr15:83612615..83814639hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38202025
hg19202025
hg18202025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2647n100
Supporting Variantsnssv3555066
Samples
Known GenesAKAP13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039043
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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