A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976133



Internal ID18611340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73099684..73101658hg38UCSC Ensembl
Innerchr13:73673822..73675796hg19UCSC Ensembl
Innerchr13:72571823..72573797hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381975
hg191975
hg181975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1968637, nssv1968641, nssv1968638, nssv1968644, nssv1968636, nssv1968640, nssv1968635, nssv1968643, nssv1968639, nssv1968642
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)nsv976133
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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