A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438241



Internal ID21095794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51558794..51569875hg38UCSC Ensembl
chr10:53318554..53329635hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3811082
hg1911082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192016
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438241
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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