A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031917



Internal ID20598957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7064636..7169216hg38UCSC Ensembl
chr16:7114637..7219217hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38104581
hg19104581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511171
Supporting Variants
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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