A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963339



Internal ID18598580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82805144..82807728hg38UCSC Ensembl
Innerchr3:82854295..82856879hg19UCSC Ensembl
Innerchr3:82936985..82939569hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg382585
hg192585
hg182585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2287090, nssv2287099, nssv2287098, nssv2287095, nssv2287097, nssv2287091, nssv2287094, nssv2287092, nssv2287096, nssv2287093
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)nsv963339
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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