A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968757



Internal ID18603985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32355..47190hg38UCSC Ensembl
Innerchr9:32355..47190hg19UCSC Ensembl
Innerchr9:22355..37190hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3814836
hg1914836
hg1814836
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2724484, nssv2724478, nssv2724480, nssv2724479, nssv2724485, nssv2724483, nssv2724486, nssv2724482, nssv2724487, nssv2724481
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM138C
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968757
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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