A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092707



Internal ID20659747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107692348..107700591hg38UCSC Ensembl
chr3:107411195..107419438hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg388244
hg198244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370250
Supporting Variants
Samples
Known GenesBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00656


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