A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534995



Internal ID20908356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47749001..47749400hg38UCSC Ensembl
chr18:45275372..45275771hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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