A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973239



Internal ID18608454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39855436..39861438hg38UCSC Ensembl
Innerchr9:42000454..42006456hg19UCSC Ensembl
Innerchr9:41990454..41996456hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386003
hg196003
hg186003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727473, nssv2727475, nssv2727470, nssv2727474, nssv2727467, nssv2727472, nssv2727476, nssv2727471, nssv2727468, nssv2727469
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP2, LOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973239
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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