A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973633



Internal ID18608848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42873077..42879163hg38UCSC Ensembl
Innerchr9:44091956..44098042hg19UCSC Ensembl
Innerchr9:44031952..44038038hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386087
hg196087
hg186087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2735580, nssv2735584, nssv2735579, nssv2735581, nssv2735582, nssv2735585, nssv2735587, nssv2735583, nssv2735588, nssv2735586
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973633
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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