A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427337



Internal ID21084890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81327201..81332200hg38UCSC Ensembl
chr8:82239436..82244435hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7396n223
Supporting Variantsnssv18223173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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