A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425699



Internal ID21083252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82628086..85182486hg38UCSC Ensembl
chr8:83540321..86094721hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg382554401
hg192554401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218899
Samples
Known GenesE2F5, LRRCC1, RALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425699
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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