A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979840



Internal ID18615041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66099363..66110529hg38UCSC Ensembl
Innerchr3:66085038..66096204hg19UCSC Ensembl
Innerchr3:66060078..66071244hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3811167
hg1911167
hg1811167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2284375, nssv2284376, nssv2284370, nssv2284377, nssv2284373, nssv2284371, nssv2284379, nssv2284374, nssv2284372, nssv2284378
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)nsv979840
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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