A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477643



Internal ID21135196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109161359..109163398hg38UCSC Ensembl
chr13:109813707..109815746hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382040
hg192040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006943
Samples
Known GenesMYO16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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