A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497921



Internal ID20871129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6730132..7040149hg38UCSC Ensembl
chr16:6780133..7090150hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38310018
hg19310018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031345
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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