A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964835



Internal ID18600071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32887729..32888346hg38UCSC Ensembl
Innerchr5:32887835..32888452hg19UCSC Ensembl
Innerchr5:32923592..32924209hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38618
hg19618
hg18618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2351751, nssv2351748, nssv2351749, nssv2351746, nssv2351747, nssv2351752, nssv2351745, nssv2351744, nssv2351743, nssv2351750
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)nsv964835
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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