A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984916



Internal ID20551957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94987453..94988130hg38UCSC Ensembl
chr10:96747210..96747887hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439544
Supporting Variants
Samples
Known GenesCYP2C9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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