A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103572



Internal ID20670612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59938130..60158421hg38UCSC Ensembl
chr3:59923856..60144149hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38220292
hg19220294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370708
Supporting Variants
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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