A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964905



Internal ID18600141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93681756..93683779hg38UCSC Ensembl
Innerchr5:93017462..93019485hg19UCSC Ensembl
Innerchr5:93043218..93045241hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382024
hg192024
hg182024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2368658, nssv2368654, nssv2368660, nssv2368655, nssv2368661, nssv2368659, nssv2368657, nssv2368656, nssv2368653, nssv2368652
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM172A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964905
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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