A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087508



Internal ID20654548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:54118771..54245247hg38UCSC Ensembl
chr2:54345908..54472384hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38126477
hg19126477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351173
Supporting Variants
Samples
Known GenesACYP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087508
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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