A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043348



Internal ID20610388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62236720..62237316hg38UCSC Ensembl
chr18:59903953..59904549hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519458
Supporting Variants
Samples
Known GenesKIAA1468
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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