A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029287



Internal ID20596327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27510309..27614403hg38UCSC Ensembl
chr16:27521630..27625724hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38104095
hg19104095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499437
Supporting Variants
Samples
Known GenesGTF3C1, KIAA0556
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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