A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450566



Internal ID21108119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51938701..51947200hg38UCSC Ensembl
chr10:53698461..53706960hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981630
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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