A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969658



Internal ID18604885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67895203..67897059hg38UCSC Ensembl
Innerchr9:67962649..67964505hg19UCSC Ensembl
Innerchr9:67552469..67554325hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381857
hg191857
hg181857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2741395, nssv2741316, nssv2741393, nssv2741386, nssv2741387, nssv2741389, nssv2741318, nssv2741321, nssv2741324, nssv2741320, nssv2741317, nssv2741394, nssv2741323, nssv2741322, nssv2741391, nssv2741319, nssv2741388, nssv2741392, nssv2741325, nssv2741390
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)nsv969658
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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