A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972399



Internal ID18607615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72106450..72108288hg38UCSC Ensembl
Innerchr9:74721366..74723204hg19UCSC Ensembl
Innerchr9:73911186..73913024hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381839
hg191839
hg181839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2551742, nssv2551737, nssv2551740, nssv2551743, nssv2551734, nssv2551735, nssv2551736, nssv2551739, nssv2551738, nssv2551741
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)nsv972399
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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