A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356721



Internal ID21014274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66457440..66459569hg38UCSC Ensembl
chr3:66507864..66509993hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382130
hg192130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102254
Samples
Known GenesLRIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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