A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953622



Internal ID36431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84806500..84806597hg38UCSC Ensembl
chr4:85727653..85727750hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454587
Supporting Variants
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953622
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0128


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