A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965187



Internal ID18600421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93931605..93932105hg38UCSC Ensembl
Innerchr3:93650449..93650949hg19UCSC Ensembl
Innerchr3:95133139..95133639hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2287893, nssv2287889, nssv2287891, nssv2287895, nssv2287898, nssv2287896, nssv2287890, nssv2287892, nssv2287894, nssv2287897
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPROS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965187
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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