A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964826



Internal ID18600062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28926610..28928964hg38UCSC Ensembl
Innerchr5:28926717..28929071hg19UCSC Ensembl
Innerchr5:28962474..28964828hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg382355
hg192355
hg182355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2351408, nssv2351406, nssv2351414, nssv2351412, nssv2351405, nssv2351407, nssv2351413, nssv2351410, nssv2351411, nssv2351409
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLSP1P3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964826
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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