A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106567



Internal ID20673607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134343753..134344481hg38UCSC Ensembl
chr4:135264908..135265636hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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