A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088550



Internal ID20655590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43261201..43271600hg38UCSC Ensembl
chr2:43488340..43498739hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343239
Supporting Variants
Samples
Known GenesTHADA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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