A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032048



Internal ID20599088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77890027..77954507hg38UCSC Ensembl
chr16:77923924..77988404hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3864481
hg1964481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505564
Supporting Variants
Samples
Known GenesVAT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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