A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977204



Internal ID18612410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21225752..21226548hg38UCSC Ensembl
Innerchr13:21799891..21800687hg19UCSC Ensembl
Innerchr13:20697891..20698687hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38797
hg19797
hg18797
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1953225, nssv1953226, nssv1953230, nssv1953229, nssv1953231, nssv1953232, nssv1953228, nssv1953233, nssv1953224, nssv1953227
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)nsv977204
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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