A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219641



Internal ID20786681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146901..66176400hg38UCSC Ensembl
chr9:42344970..42374365hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3829500
hg1929396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444423
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00078


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