A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029140



Internal ID20596180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30056345..30071415hg38UCSC Ensembl
chr16:30067666..30082736hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3815071
hg1915071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500043
Supporting Variants
Samples
Known GenesALDOA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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