A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445864



Internal ID21103417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51063131..51063648hg38UCSC Ensembl
chr10:52822891..52823408hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981530
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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