A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950153



Internal ID34119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56516692..56525561hg38UCSC Ensembl
chr4:57382858..57391727hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg388870
hg198870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466435
Supporting Variants
Samples
Known GenesARL9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950153
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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