A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017003



Internal ID21926346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95269479..95271338hg38UCSC Ensembl
chr10:97029236..97031095hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381860
hg191860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578069
Samples
Known GenesPDLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017003
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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