A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957140



Internal ID38740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153369644..153372437hg38UCSC Ensembl
chr4:154290796..154293589hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460741
Supporting Variants
Samples
Known GenesMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957140
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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