A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984587



Internal ID20551627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84222081..84222561hg38UCSC Ensembl
chr10:85981837..85982317hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441083
Supporting Variants
Samples
Known GenesLRIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00159


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