A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087253



Internal ID20654293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:51097663..51391137hg38UCSC Ensembl
chr2:51324801..51618275hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38293475
hg19293475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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