A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981156



Internal ID20548196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26193820..26194159hg38UCSC Ensembl
chr10:26482749..26483088hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440015
Supporting Variants
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00137


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