A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260720



Internal ID20469938
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 StatusS
Merged Variantsnsv4740845
Supporting Variants
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260720
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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