A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586652



Internal ID21535207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33554461..33554517hg38UCSC Ensembl
chr19:34045367..34045423hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104777
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586652
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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