A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087386



Internal ID20654426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235076433..235076703hg38UCSC Ensembl
chr2:235985077..235985347hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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