A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050679



Internal ID19139898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85268380..85567625hg38UCSC Ensembl
Innerchr15:85811611..86110856hg19UCSC Ensembl
Innerchr15:83612615..83911860hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38299246
hg19299246
hg18299246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2648n100
Supporting Variantsnssv3718142
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)nsv1050679
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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