A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497968



Internal ID20871176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68199204..68209317hg38UCSC Ensembl
chr16:68233107..68243220hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3810114
hg1910114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191533
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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