A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945559



Internal ID31035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16726455..16726499hg38UCSC Ensembl
chr4:16728078..16728122hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409365
Supporting Variants
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945559
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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