A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528402



Internal ID20901763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62230671..62231048hg38UCSC Ensembl
chr18:59897904..59898281hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043346
Samples
Known GenesKIAA1468
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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