A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973707



Internal ID18608922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63977698..63979086hg38UCSC Ensembl
Innerchr9:69221118..69222512hg19UCSC Ensembl
Innerchr9:68510938..68512332hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381389
hg191395
hg181395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2743359, nssv2743363, nssv2743362, nssv2743360, nssv2743358, nssv2743355, nssv2743357, nssv2743356, nssv2743354, nssv2743361
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973707
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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