A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079839



Internal ID20646879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158169033..158169673hg38UCSC Ensembl
chr2:159025545..159026185hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341754
Supporting Variants
Samples
Known GenesCCDC148-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079839
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00058


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