A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209585



Internal ID20776625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134826002..135256433hg38UCSC Ensembl
chr3:134544844..134975275hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38430432
hg19430432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363581
Supporting Variants
Samples
Known GenesEPHB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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