A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977733



Internal ID18612939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72896897..72900430hg38UCSC Ensembl
Innerchr15:73189238..73192771hg19UCSC Ensembl
Innerchr15:70976291..70979824hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383534
hg193534
hg183534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2031548, nssv2031550, nssv2031544, nssv2031541, nssv2031549, nssv2031542, nssv2031547, nssv2031543, nssv2031545, nssv2031546
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977733
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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