A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974076



Internal ID18609289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31482966..31483466hg38UCSC Ensembl
Innerchr13:32057103..32057603hg19UCSC Ensembl
Innerchr13:30955103..30955603hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1959097, nssv1959101, nssv1959096, nssv1959100, nssv1959103, nssv1959099, nssv1959095, nssv1959102, nssv1959098, nssv1959094
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)nsv974076
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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