A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969656



Internal ID18604883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67888862..67890085hg38UCSC Ensembl
Innerchr9:67956165..67957531hg19UCSC Ensembl
Innerchr9:67545985..67547351hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381224
hg191367
hg181367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2739718, nssv2739714, nssv2739711, nssv2739719, nssv2739715, nssv2739717, nssv2739712, nssv2739710, nssv2739713, nssv2739716
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969656
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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