A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077879



Internal ID20644920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135246867..135311730hg38UCSC Ensembl
chr2:136004437..136069300hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg3864864
hg1964864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346478
Supporting Variants
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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