A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532128



Internal ID20905489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59912785..59943364hg38UCSC Ensembl
chr18:57580017..57610596hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3830580
hg1930580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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