A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030000



Internal ID20597040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50161634..50194757hg38UCSC Ensembl
chr16:50195545..50228668hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3833124
hg1933124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504897
Supporting Variants
Samples
Known GenesPAPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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