A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520547



Internal ID20893908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56089201..56123400hg38UCSC Ensembl
chr18:53756432..53790631hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3834200
hg1934200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3376n223
Supporting Variantsnssv18042547
Samples
Known GenesLOC100505474
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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