A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444846



Internal ID21102399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51044145..51404106hg38UCSC Ensembl
chr10:52803905..53163866hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38359962
hg19359962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193477
Samples
Known GenesMIR605, PRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444846
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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