A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437665



Internal ID21095218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68780692..69356266hg38UCSC Ensembl
chr9:71395608..71971182hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38575575
hg19575575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224634
Samples
Known GenesBANCR, FAM122A, FAM189A2, FXN, PIP5K1B, PRKACG, TJP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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