A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206210



Internal ID20773250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231578191..231639778hg38UCSC Ensembl
chr2:232442902..232504489hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3861588
hg1961588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350843
Supporting Variants
Samples
Known GenesC2orf57
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206210
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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