A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098135



Internal ID20665175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167637501..167639600hg38UCSC Ensembl
chr3:167355289..167357388hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357319
Supporting Variants
Samples
Known GenesWDR49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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