A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967072



Internal ID18602301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138824354..138832005hg38UCSC Ensembl
Innerchr3:138543196..138550847hg19UCSC Ensembl
Innerchr3:140025886..140033537hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg387652
hg197652
hg187652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2299050, nssv2299045, nssv2299049, nssv2299046, nssv2299051, nssv2299043, nssv2299047, nssv2299048, nssv2299052, nssv2299044
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)nsv967072
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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