A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052259



Internal ID19141478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85268380..85569198hg38UCSC Ensembl
Innerchr15:85811611..86112429hg19UCSC Ensembl
Innerchr15:83612615..83913433hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38300819
hg19300819
hg18300819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2648n100
Supporting Variantsnssv3555068, nssv3555067
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)nsv1052259
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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