A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085156



Internal ID20652196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241641701..241642500hg38UCSC Ensembl
chr2:242581116..242581915hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347034
Supporting Variants
Samples
Known GenesATG4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01247


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