A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726851



Internal ID150517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38730111..38740955hg38UCSC Ensembl
chr21:40102035..40112879hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3810845
hg1910845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540805
Supporting Variants
Samples
Known GenesLINC00114
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726851
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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