A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534074



Internal ID309926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95139864..95139874hg38UCSC Ensembl
chr9:97902146..97902156hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025835
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534074
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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