A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491521



Internal ID268758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96506924..96508281hg38UCSC Ensembl
chr8:97519152..97520509hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381358
hg191358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016117
Samples
Known GenesSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491521
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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