A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005392



Internal ID21914735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96643989..96647789hg38UCSC Ensembl
chr8:97656217..97660017hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383801
hg193801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580737
Samples
Known GenesCPQ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005392
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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