A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982424



Internal ID18617619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64395637..64396335hg38UCSC Ensembl
Innerchr9:43106777..43107475hg19UCSC Ensembl
Innerchr9:43096773..43097471hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38699
hg19699
hg18699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2732134, nssv2732139, nssv2732194, nssv2732136, nssv2732196, nssv2732133, nssv2732192, nssv2732198, nssv2732141, nssv2732197, nssv2732137, nssv2732193, nssv2732132, nssv2732190, nssv2732191, nssv2732199, nssv2732138, nssv2732135, nssv2732195, nssv2732140
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)nsv982424
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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