A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974080



Internal ID18609293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:35309558..35310518hg38UCSC Ensembl
Innerchr13:35883695..35884655hg19UCSC Ensembl
Innerchr13:34781695..34782655hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38961
hg19961
hg18961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1959503, nssv1959501, nssv1959507, nssv1959506, nssv1959505, nssv1959502, nssv1959504, nssv1959509, nssv1959500, nssv1959508
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)nsv974080
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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