A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969588



Internal ID18604815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42912353..42924051hg38UCSC Ensembl
Innerchr9:44047068..44058766hg19UCSC Ensembl
Innerchr9:43987064..43998762hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811699
hg1911699
hg1811699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2734102, nssv2734098, nssv2734101, nssv2734103, nssv2734097, nssv2734104, nssv2734099, nssv2734100, nssv2734096, nssv2734095
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)nsv969588
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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