A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106029



Internal ID20673069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85821089..85821494hg38UCSC Ensembl
chr3:85870239..85870644hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358579
Supporting Variants
Samples
Known GenesCADM2, CADM2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00211


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