A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526828



Internal ID20900189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49398647..49406004hg38UCSC Ensembl
chr18:46925017..46932374hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg387358
hg197358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042140
Samples
Known GenesDYM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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