A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036782



Internal ID21946125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75032693..75032894hg38UCSC Ensembl
chr18:72744649..72744850hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634252
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036782
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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