A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079182



Internal ID20646222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155757601..155759600hg38UCSC Ensembl
chr2:156614113..156616112hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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