A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977226



Internal ID18612432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37992392..37994305hg38UCSC Ensembl
Innerchr13:38566529..38568442hg19UCSC Ensembl
Innerchr13:37464529..37466442hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381914
hg191914
hg181914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1959981, nssv1959980, nssv1959987, nssv1959986, nssv1959983, nssv1959984, nssv1959989, nssv1959982, nssv1959988, nssv1959985
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)nsv977226
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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