A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087981



Internal ID20655021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52056601..52131700hg38UCSC Ensembl
chr2:52283739..52358838hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3875100
hg1975100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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