A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976102



Internal ID18611309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:35054357..35055774hg38UCSC Ensembl
Innerchr13:35628494..35629911hg19UCSC Ensembl
Innerchr13:34526494..34527911hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381418
hg191418
hg181418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1960361, nssv1960355, nssv1960363, nssv1960360, nssv1960362, nssv1960356, nssv1960357, nssv1960354, nssv1960358, nssv1960359
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNBEA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976102
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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