A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962481



Internal ID18597724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3017853..3026993hg38UCSC Ensembl
Innerchr18:3017851..3026991hg19UCSC Ensembl
Innerchr18:3007851..3016991hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg389141
hg199141
hg189141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2112394, nssv2112400, nssv2112392, nssv2112393, nssv2112395, nssv2112397, nssv2112401, nssv2112399, nssv2112398, nssv2112396
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)nsv962481
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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