A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965851



Internal ID44560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64991231..64991424hg38UCSC Ensembl
chr5:64287058..64287251hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467199
Supporting Variants
Samples
Known GenesCWC27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965851
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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