A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083036



Internal ID20650076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213197522..213204808hg38UCSC Ensembl
chr2:214062246..214069532hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg387287
hg197287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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