A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734092



Internal ID157758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15055015..15056967hg38UCSC Ensembl
chr21:16427336..16429288hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381953
hg191953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528264
Supporting Variants
Samples
Known GenesNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734092
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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