A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905540



Internal ID4502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85264947..85265108hg38UCSC Ensembl
chr1:85730630..85730791hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905540
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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