A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101463



Internal ID20668503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63835583..63836030hg38UCSC Ensembl
chr3:63821259..63821706hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363146
Supporting Variants
Samples
Known GenesC3orf49, THOC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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