A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972406



Internal ID18607622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82130981..82132840hg38UCSC Ensembl
Innerchr9:84745896..84747755hg19UCSC Ensembl
Innerchr9:83935716..83937575hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381860
hg191860
hg181860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555212, nssv2555209, nssv2555207, nssv2555205, nssv2555213, nssv2555206, nssv2555210, nssv2555208, nssv2555204, nssv2555211
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972406
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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