A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957511



Internal ID38985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139026496..139027182hg38UCSC Ensembl
chr4:139947650..139948336hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462513
Supporting Variants
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.14986


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