A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984954



Internal ID20551995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89403961..89412978hg38UCSC Ensembl
chr10:91163718..91172735hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg389018
hg199018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448463
Supporting Variants
Samples
Known GenesIFIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984954
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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