A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075586



Internal ID20642626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112960556..113135775hg38UCSC Ensembl
chr2:113718133..113893352hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38175220
hg19175220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343530
Supporting Variants
Samples
Known GenesIL1F10, IL1RN, IL36A, IL36B, IL36G, IL36RN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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