A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094831



Internal ID20661871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134514448..134514810hg38UCSC Ensembl
chr3:134233290..134233652hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361862
Supporting Variants
Samples
Known GenesCEP63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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