A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632756



Internal ID21824803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54167724..54167869hg38UCSC Ensembl
chr18:51694094..51694239hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024554
Supporting Variants
Samples
Known GenesMBD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632756
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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