A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093099



Internal ID20660139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105486144..105630246hg38UCSC Ensembl
chr3:105204988..105349090hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38144103
hg19144103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358714
Supporting Variants
Samples
Known GenesALCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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