A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948727



Internal ID33179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32069358..32069358hg38UCSC Ensembl
chr4:32070980..32070980hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948727
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.318927


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