A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984332



Internal ID20551373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77405879..77426757hg38UCSC Ensembl
chr10:79165637..79186515hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3820879
hg1920879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452552
Supporting Variants
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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