A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973238



Internal ID18608453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39844406..39855436hg38UCSC Ensembl
Innerchr9:41989424..42000454hg19UCSC Ensembl
Innerchr9:41979424..41990454hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3811031
hg1911031
hg1811031
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727457, nssv2727460, nssv2727461, nssv2727455, nssv2727463, nssv2727462, nssv2727459, nssv2727464, nssv2727456, nssv2727458
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP2
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973238
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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