A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096324



Internal ID20663365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149573284..149583804hg38UCSC Ensembl
chr3:149291071..149301591hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3810521
hg1910521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370127
Supporting Variants
Samples
Known GenesWWTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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