A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977255



Internal ID18612461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67266863..67270590hg38UCSC Ensembl
Innerchr13:67840995..67844722hg19UCSC Ensembl
Innerchr13:66738996..66742723hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg383728
hg193728
hg183728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1968432, nssv1968436, nssv1968434, nssv1968433, nssv1968441, nssv1968435, nssv1968440, nssv1968438, nssv1968437, nssv1968439
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)nsv977255
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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