A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272315



Internal ID20481533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53885117..53885193hg38UCSC Ensembl
chr18:51411487..51411563hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272315
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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