A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951955



Internal ID35324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95933687..95997572hg38UCSC Ensembl
chr4:96854838..96918723hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3863886
hg1963886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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