A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042620



Internal ID19131839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85745502..85773712hg38UCSC Ensembl
Innerchr15:86288733..86316943hg19UCSC Ensembl
Innerchr15:84089737..84117947hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3828211
hg1928211
hg1828211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2649n100
Supporting Variantsnssv3555079
Samples
Known GenesAKAP13, KLHL25, MIR1276
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042620
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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