A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600747



Internal ID21549388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54224630..54244412hg38UCSC Ensembl
chr19:54728504..54748253hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819783
hg1919750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106085
SamplesNA19238
Known GenesLILRA6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600747
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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