A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101257



Internal ID20668297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19476080..19476646hg38UCSC Ensembl
chr3:19517572..19518138hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359615
Supporting Variants
Samples
Known GenesKCNH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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