A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962877



Internal ID18598119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41786617..41789569hg38UCSC Ensembl
Innerchr18:39366582..39369534hg19UCSC Ensembl
Innerchr18:37620580..37623532hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382953
hg192953
hg182953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2121883, nssv2121885, nssv2121882, nssv2121890, nssv2121887, nssv2121886, nssv2121884, nssv2121889, nssv2121888, nssv2121891
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)nsv962877
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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