A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079824



Internal ID20646864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157944161..157950374hg38UCSC Ensembl
chr2:158800673..158806886hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg386214
hg196214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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