A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087952



Internal ID20654992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:51873859..51928112hg38UCSC Ensembl
chr2:52100997..52155250hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3854254
hg1954254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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