A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918620



Internal ID22693841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97841815..97841864hg38UCSC Ensembl
chr10:99601572..99601621hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363681
Samples
Known GenesLINC00866
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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