A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984952



Internal ID20551993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89381814..89442315hg38UCSC Ensembl
chr10:91141571..91202072hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3860502
hg1960502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454393
Supporting Variants
Samples
Known GenesIFIT1, IFIT1B, IFIT5, SLC16A12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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