A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002309



Internal ID21911652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143015576..143015753hg38UCSC Ensembl
chr8:144096993..144097170hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585730
Samples
Known GenesLOC100133669
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002309
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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