A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499732



Internal ID20872955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3913679..4154253hg38UCSC Ensembl
chr16:3963680..4204254hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38240575
hg19240575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181466
Samples
Known GenesADCY9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499732
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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