A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446061



Internal ID21103614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87557689..87561275hg38UCSC Ensembl
chr9:90172604..90176190hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383587
hg193587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190768
Samples
Known GenesDAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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