A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517652



Internal ID20891013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74772093..74773901hg38UCSC Ensembl
chr18:72484049..72485857hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043945
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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