A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532494



Internal ID20905855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74906295..74909769hg38UCSC Ensembl
chr18:72618251..72621725hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg383475
hg193475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043970
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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