A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896976



Internal ID172140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209681475..209683407hg38UCSC Ensembl
chr1:209854820..209856752hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381933
hg191933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445175
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896976
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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