A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983576



Internal ID18618769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37406339..37408364hg38UCSC Ensembl
Innerchr13:37980476..37982501hg19UCSC Ensembl
Innerchr13:36878476..36880501hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382026
hg192026
hg182026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1959890, nssv1959887, nssv1959892, nssv1959891, nssv1959885, nssv1959889, nssv1959884, nssv1958827, nssv1959888, nssv1959886
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)nsv983576
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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