A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721469



Internal ID145135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12053727..12066782hg38UCSC Ensembl
chr19:12164542..12177597hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813056
hg1913056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523680
Supporting Variants
Samples
Known GenesZNF844
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721469
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.012648


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