A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048308



Internal ID19137527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85268380..85597248hg38UCSC Ensembl
Innerchr15:85811611..86140479hg19UCSC Ensembl
Innerchr15:83612615..83941483hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38328869
hg19328869
hg18328869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2648n100
Supporting Variantsnssv3718143, nssv3555070, nssv3555069, nssv3718146, nssv3718145, nssv3718144, nssv3555071
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)nsv1048308
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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