A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018325



Internal ID21927668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178156308..178196541hg38UCSC Ensembl
chr5:177583309..177623542hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3840234
hg1940234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570144
Samples
Known GenesGMCL1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018325
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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