A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028220



Internal ID21937563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45593111..45593255hg38UCSC Ensembl
chr18:43173076..43173220hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630904
Samples
Known GenesSLC14A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028220
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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