A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974595



Internal ID18609806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71163690..71166029hg38UCSC Ensembl
Innerchr15:71456029..71458368hg19UCSC Ensembl
Innerchr15:69243083..69245422hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382340
hg192340
hg182340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2029275, nssv2029268, nssv2029272, nssv2029270, nssv2029273, nssv2029276, nssv2029269, nssv2029277, nssv2029271, nssv2029274
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTHSD4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974595
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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