A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968616



Internal ID18257158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37886803..37889873hg38UCSC Ensembl
Innerchr9:37886800..37889870hg19UCSC Ensembl
Innerchr9:37876800..37879870hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383071
hg193071
hg183071
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2530579, nssv2530581, nssv2530583, nssv2530586, nssv2530587, nssv2530582, nssv2530578, nssv2530584, nssv2530585, nssv2530580
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSLC25A51
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968616
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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