A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972432



Internal ID18607648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97112325..97195813hg38UCSC Ensembl
Innerchr9:99874607..99958095hg19UCSC Ensembl
Innerchr9:98914428..98997916hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3883489
hg1983489
hg1883489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561052, nssv2561054, nssv2561057, nssv2561058, nssv2561053, nssv2561060, nssv2561056, nssv2561051, nssv2561059, nssv2561055
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)nsv972432
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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