A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889201



Internal ID166892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150915788..150917752hg38UCSC Ensembl
chr1:150888264..150890228hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381965
hg191965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889201
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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