A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493168



Internal ID21150721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39704040..39704623hg38UCSC Ensembl
chr13:40278177..40278760hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008723
Samples
Known GenesCOG6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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