A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969570



Internal ID18604797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64407781..64412274hg38UCSC Ensembl
Innerchr9:43090842..43095332hg19UCSC Ensembl
Innerchr9:43080838..43085328hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384494
hg194491
hg184491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2731082, nssv2731086, nssv2731083, nssv2731080, nssv2731084, nssv2731087, nssv2731085, nssv2731081, nssv2731088, nssv2731089
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969570
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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