A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972348



Internal ID18607564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42740370..42803552hg38UCSC Ensembl
Innerchr9:44167567..44230749hg19UCSC Ensembl
Innerchr9:44107563..44170745hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3863183
hg1963183
hg1863183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2539063, nssv2539057, nssv2539061, nssv2539065, nssv2539060, nssv2539056, nssv2539062, nssv2539059, nssv2539064, nssv2539058
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)nsv972348
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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