A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962900



Internal ID18598142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14884984..14891899hg38UCSC Ensembl
Innerchr18:14884983..14891898hg19UCSC Ensembl
Innerchr18:14874983..14881898hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg386916
hg196916
hg186916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv40n82
Supporting Variantsnssv2658460, nssv2658465, nssv2658461, nssv2658464, nssv2658463, nssv2658457, nssv2657840, nssv2658462, nssv2658458, nssv2658459
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962900
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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