A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088692



Internal ID20655732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44981862..45081745hg38UCSC Ensembl
chr2:45209001..45308884hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3899884
hg1999884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339100
Supporting Variants
Samples
Known GenesSIX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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