A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261788



Internal ID20471006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25853210..25853268hg38UCSC Ensembl
chr18:23433174..23433232hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261788
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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