A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077880



Internal ID20644921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135321222..135330133hg38UCSC Ensembl
chr2:136078792..136087703hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg388912
hg198912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343945
Supporting Variants
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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