A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967689



Internal ID45768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43085459..43089179hg38UCSC Ensembl
chr5:43085561..43089281hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg383721
hg193721
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429934
Supporting Variants
Samples
Known GenesLOC100506639
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967689
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.499027


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