A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965218



Internal ID18600452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141861732..141865587hg38UCSC Ensembl
Innerchr3:141580574..141584429hg19UCSC Ensembl
Innerchr3:143063264..143067119hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383856
hg193856
hg183856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2297723, nssv2297721, nssv2297716, nssv2297718, nssv2297717, nssv2297715, nssv2297722, nssv2297719, nssv2297720, nssv2297724
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)nsv965218
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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