A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740845



Internal ID20516822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76895850..76895943hg38UCSC Ensembl
chr18:74607806..74607899hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260720
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740845
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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