A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018205



Internal ID21927548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143342195..143342572hg38UCSC Ensembl
chr8:144424365..144424742hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585424
Samples
Known GenesTOP1MT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018205
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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