A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104127



Internal ID21442532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22652221..22652387hg38UCSC Ensembl
chr19:22835023..22835189hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597466
Supporting Variants
SamplesHG00732
Known GenesZNF492
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104127
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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