A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082994



Internal ID20650034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212912996..212913676hg38UCSC Ensembl
chr2:213777720..213778400hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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