A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001897



Internal ID21911240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130854793..130854860hg38UCSC Ensembl
chr8:131867039..131867106hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585589
Samples
Known GenesADCY8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001897
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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