A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102799



Internal ID20669839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55966946..55968282hg38UCSC Ensembl
chr3:56000974..56002310hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362488
Supporting Variants
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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