A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528612



Internal ID22398001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:134144459..134144776hg38UCSC Ensembl
chr8:135156702..135157019hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14344063, nssv14344064
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528612
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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