A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004472



Internal ID21913815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132980581..132980927hg38UCSC Ensembl
chr8:133992826..133993172hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594608
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004472
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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