A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085081



Internal ID20652121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209823092..209823716hg38UCSC Ensembl
chr2:210687816..210688440hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345557
Supporting Variants
Samples
Known GenesUNC80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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