A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972803



Internal ID18608019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121510969..121529102hg38UCSC Ensembl
Innerchr9:124273248..124291381hg19UCSC Ensembl
Innerchr9:123313069..123331202hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3818134
hg1918134
hg1818134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2565856, nssv2565853, nssv2565858, nssv2565852, nssv2565850, nssv2565855, nssv2565854, nssv2565849, nssv2565857, nssv2565851
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)nsv972803
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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