A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981154



Internal ID20548194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26167901..26177700hg38UCSC Ensembl
chr10:26456830..26466629hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448499
Supporting Variants
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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