A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946516



Internal ID31712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17304735..17305816hg38UCSC Ensembl
chr4:17306358..17307439hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946516
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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