A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145226



Internal ID20712266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75780018..75782718hg38UCSC Ensembl
chr6:76489735..76492435hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382701
hg192701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399524
Supporting Variants
Samples
Known GenesMYO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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