A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030829



Internal ID20597869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67738707..67739221hg38UCSC Ensembl
chr16:67772610..67773124hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509270
Supporting Variants
Samples
Known GenesRANBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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