A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502644



Internal ID20875890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7348203..7770511hg38UCSC Ensembl
chr16:7398204..7820513hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38422309
hg19422310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183135
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502644
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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