A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953624



Internal ID36433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84869834..84869887hg38UCSC Ensembl
chr4:85790987..85791040hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472029
Supporting Variants
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953624
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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