A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102787



Internal ID20669827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55790287..55790848hg38UCSC Ensembl
chr3:55824315..55824876hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371413
Supporting Variants
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00075


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