A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502909



Internal ID20876158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69618545..69625017hg38UCSC Ensembl
chr16:69652448..69658920hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386473
hg196473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031222
Samples
Known GenesNFAT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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