A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969596



Internal ID18604823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42842189..42845119hg38UCSC Ensembl
Innerchr9:44126000..44128930hg19UCSC Ensembl
Innerchr9:44065996..44068926hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382931
hg192931
hg182931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2736052, nssv2736113, nssv2736104, nssv2736107, nssv2736047, nssv2736050, nssv2736109, nssv2736105, nssv2736051, nssv2736055, nssv2736046, nssv2736112, nssv2736048, nssv2736108, nssv2736054, nssv2736053, nssv2736049, nssv2736111, nssv2736106, nssv2736110
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)nsv969596
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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