A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965186



Internal ID18600420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93930326..93931605hg38UCSC Ensembl
Innerchr3:93649170..93650449hg19UCSC Ensembl
Innerchr3:95131860..95133139hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg381280
hg191280
hg181280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2287794, nssv2287796, nssv2287800, nssv2287797, nssv2287799, nssv2287798, nssv2287793, nssv2287792, nssv2287795, nssv2287801
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)nsv965186
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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