A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974079



Internal ID18609292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34927805..34929206hg38UCSC Ensembl
Innerchr13:35501942..35503343hg19UCSC Ensembl
Innerchr13:34399942..34401343hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381402
hg191402
hg181402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1960160, nssv1960161, nssv1960165, nssv1960162, nssv1960169, nssv1960167, nssv1960168, nssv1960164, nssv1960163, nssv1960166
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)nsv974079
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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