A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982192



Internal ID18617387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2892906..2900752hg38UCSC Ensembl
Innerchr9:2892906..2900752hg19UCSC Ensembl
Innerchr9:2882906..2890752hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg387847
hg197847
hg187847
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2519852, nssv2519854, nssv2519853, nssv2519849, nssv2519851, nssv2519845, nssv2519846, nssv2519847, nssv2519850, nssv2519848
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)nsv982192
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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