A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522838



Internal ID20896199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56524725..56581962hg38UCSC Ensembl
chr18:54191956..54249193hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3857238
hg1957238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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