A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946232



Internal ID31512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20577865..20578390hg38UCSC Ensembl
chr4:20579488..20580013hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451097
Supporting Variants
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946232
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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