A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444113



Internal ID21101666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113765301..113770800hg38UCSC Ensembl
chr10:115525060..115530559hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977668
Samples
Known GenesPLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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