A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023505



Internal ID21932848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50946270..50946503hg38UCSC Ensembl
chr18:48472640..48472873hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623182
Samples
Known GenesME2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023505
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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