A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977236



Internal ID18612442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:45436234..45436913hg38UCSC Ensembl
Innerchr13:46010369..46011048hg19UCSC Ensembl
Innerchr13:44908370..44909049hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38680
hg19680
hg18680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1962394, nssv1962402, nssv1962401, nssv1962398, nssv1962400, nssv1962395, nssv1962399, nssv1962393, nssv1962397, nssv1962396
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)nsv977236
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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