A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518338



Internal ID20891699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62233417..62234145hg38UCSC Ensembl
chr18:59900650..59901378hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043347
Samples
Known GenesKIAA1468
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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