A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530581



Internal ID20903942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:52633056..52655711hg38UCSC Ensembl
chr18:50159426..50182081hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3822656
hg1922656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041576
Samples
Known GenesDCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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