A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079138



Internal ID20646179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156153174..156153919hg38UCSC Ensembl
chr2:157009686..157010431hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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