A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967114



Internal ID18602343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75842865..75851790hg38UCSC Ensembl
Innerchr3:75892016..75900941hg19UCSC Ensembl
Innerchr3:75974706..75983631hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg388926
hg198926
hg188926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2693879, nssv2693881, nssv2693873, nssv2693878, nssv2693876, nssv2693875, nssv2693880, nssv2693877, nssv2693874, nssv2693872
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967114
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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