A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032126



Internal ID20599166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7385473..7522074hg38UCSC Ensembl
chr16:7435474..7572076hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38136602
hg19136603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501272
Supporting Variants
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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