A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439765



Internal ID21097318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52070003..52231777hg38UCSC Ensembl
chr10:53829763..53991537hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38161775
hg19161775
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178811
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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