A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598962



Internal ID21547594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56114373..56114422hg38UCSC Ensembl
chr19:56625742..56625791hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106306
SamplesHG03065
Known GenesZNF787
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598962
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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