A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977765



Internal ID18612971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101955269..101969546hg38UCSC Ensembl
Innerchr15:102495472..102509749hg19UCSC Ensembl
Innerchr15:100312995..100327272hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3814278
hg1914278
hg1814278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2040590, nssv2040589, nssv2040588, nssv2040596, nssv2040595, nssv2040594, nssv2040593, nssv2040587, nssv2040592, nssv2040591
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM138E, WASH3P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977765
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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