A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443821



Internal ID21101374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128057467..128060457hg38UCSC Ensembl
chr10:129855731..129858721hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382991
hg192991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978833
Samples
Known GenesPTPRE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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