A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016320



Internal ID21925663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124546294..124546862hg38UCSC Ensembl
chr10:126234863..126235431hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596961
Samples
Known GenesLHPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016320
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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