A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972717



Internal ID18607933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42621793..42631840hg38UCSC Ensembl
Innerchr9:44298592..44308643hg19UCSC Ensembl
Innerchr9:44238588..44248639hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810048
hg1910052
hg1810052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2539292, nssv2539298, nssv2539297, nssv2539291, nssv2539294, nssv2539295, nssv2539289, nssv2539296, nssv2539290, nssv2539293
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)nsv972717
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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