A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968739



Internal ID18603967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100116799..100120602hg38UCSC Ensembl
Innerchr9:102879081..102882884hg19UCSC Ensembl
Innerchr9:101918902..101922705hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg383804
hg193804
hg183804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2562305, nssv2562299, nssv2562302, nssv2562306, nssv2562300, nssv2562298, nssv2562303, nssv2562304, nssv2562301, nssv2562297
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesINVS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968739
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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