A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905909



Internal ID4739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87359241..87359241hg38UCSC Ensembl
chr1:87824924..87824924hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541244
Supporting Variants
Samples
Known GenesLOC100505768
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905909
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007805


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