A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366425



Internal ID21023978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85461781..85563462hg38UCSC Ensembl
chr3:85510931..85612612hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38101682
hg19101682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4936n223
Supporting Variantsnssv18105971
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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