A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969594



Internal ID18604821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42896180..42897018hg38UCSC Ensembl
Innerchr9:44074101..44074939hg19UCSC Ensembl
Innerchr9:44014097..44014935hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38839
hg19839
hg18839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2732718, nssv2733581, nssv2732721, nssv2733583, nssv2733582, nssv2732722, nssv2733584, nssv2732717, nssv2732787, nssv2732724, nssv2732786, nssv2732715, nssv2732719, nssv2733586, nssv2732716, nssv2733585, nssv2732723, nssv2732720, nssv2732785, nssv2733580
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969594
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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