A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982362



Internal ID18617557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5109925..5110532hg38UCSC Ensembl
Innerchr9:5109925..5110532hg19UCSC Ensembl
Innerchr9:5099925..5100532hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38608
hg19608
hg18608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2725712, nssv2725720, nssv2725713, nssv2725718, nssv2725714, nssv2725715, nssv2725716, nssv2725711, nssv2725719, nssv2725717
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesJAK2
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982362
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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