A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962501



Internal ID18597744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22586533..22587033hg38UCSC Ensembl
Innerchr18:20166496..20166996hg19UCSC Ensembl
Innerchr18:18420494..18420994hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2118963, nssv2118961, nssv2118968, nssv2118965, nssv2118966, nssv2118970, nssv2118962, nssv2118969, nssv2118967, nssv2118964
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)nsv962501
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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