A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952383



Internal ID35613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76855770..76855821hg38UCSC Ensembl
chr4:77776923..77776974hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952383
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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