A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437862



Internal ID21095415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110769696..110782248hg38UCSC Ensembl
chr9:113531976..113544528hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3812553
hg1912553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173246
Samples
Known GenesMUSK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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