A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965176



Internal ID18600410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75346016..75619904hg38UCSC Ensembl
Innerchr3:75395167..75669055hg19UCSC Ensembl
Innerchr3:75477857..75751745hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38273889
hg19273889
hg18273889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2283747, nssv2283752, nssv2283750, nssv2283749, nssv2283755, nssv2283746, nssv2283754, nssv2283751, nssv2283753, nssv2283748
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM86DP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965176
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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