A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965178



Internal ID18600412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75871779..75879929hg38UCSC Ensembl
Innerchr3:75920930..75929080hg19UCSC Ensembl
Innerchr3:76003620..76011770hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg388151
hg198151
hg188151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2284151, nssv2284149, nssv2284146, nssv2284150, nssv2284152, nssv2284147, nssv2284143, nssv2284148, nssv2284145, nssv2284144
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)nsv965178
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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