A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015683



Internal ID21925026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97841827..97841884hg38UCSC Ensembl
chr10:99601584..99601641hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584652
Samples
Known GenesLINC00866
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015683
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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