A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082963



Internal ID20650003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206443201..206445000hg38UCSC Ensembl
chr2:207307925..207309724hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355254
Supporting Variants
Samples
Known GenesADAM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01982


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