A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119654



Internal ID20686694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84806499..84806597hg38UCSC Ensembl
chr4:85727652..85727750hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389581
Supporting Variants
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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