A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977753



Internal ID18612959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85771028..85771790hg38UCSC Ensembl
Innerchr15:86314259..86315021hg19UCSC Ensembl
Innerchr15:84115263..84116025hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38763
hg19763
hg18763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2036545, nssv2036547, nssv2036543, nssv2036544, nssv2036548, nssv2036541, nssv2036540, nssv2036542, nssv2036546, nssv2036549
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKLHL25
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977753
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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