A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591066



Internal ID21539638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12053911..12066781hg38UCSC Ensembl
chr19:12164726..12177596hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812871
hg1912871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103129
SamplesHG01596
Known GenesZNF844
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591066
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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