A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967052



Internal ID18602281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112301589..112309090hg38UCSC Ensembl
Innerchr3:112020436..112027937hg19UCSC Ensembl
Innerchr3:113503126..113510627hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg387502
hg197502
hg187502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2288913, nssv2288910, nssv2288912, nssv2288917, nssv2288911, nssv2288909, nssv2288916, nssv2288915, nssv2288918, nssv2288914
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)nsv967052
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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