A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116699



Internal ID20683739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32683601..32685400hg38UCSC Ensembl
chr4:32685223..32687022hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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