A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448997



Internal ID21106550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68885222..69216232hg38UCSC Ensembl
chr9:71500138..71831148hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38331011
hg19331011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222332
Samples
Known GenesFXN, PIP5K1B, PRKACG, TJP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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