A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972466



Internal ID18607682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135072..135670hg38UCSC Ensembl
Innerchr9:135072..135670hg19UCSC Ensembl
Innerchr9:125072..125670hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38599
hg19599
hg18599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2725666, nssv2725668, nssv2725670, nssv2725667, nssv2725672, nssv2725675, nssv2725673, nssv2725671, nssv2725674, nssv2725669
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972466
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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