A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100826



Internal ID20667866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38351198..38358210hg38UCSC Ensembl
chr3:38392689..38399701hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387013
hg197013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356080
Supporting Variants
Samples
Known GenesXYLB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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