A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960646



Internal ID18595893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4998726..5003191hg38UCSC Ensembl
Innerchr18:4998725..5003190hg19UCSC Ensembl
Innerchr18:4988725..4993190hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg384466
hg194466
hg184466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2114322, nssv2114328, nssv2114321, nssv2114326, nssv2114327, nssv2114320, nssv2114323, nssv2114324, nssv2114325, nssv2114319
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)nsv960646
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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