A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030009



Internal ID20597049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5039154..5040309hg38UCSC Ensembl
chr16:5089155..5090310hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515186
Supporting Variants
Samples
Known GenesNAGPA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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