A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951863



Internal ID35271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94416787..94416838hg38UCSC Ensembl
chr4:95337938..95337989hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951863
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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