A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028474



Internal ID20595514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14835901..14836900hg38UCSC Ensembl
chr16:14929758..14930757hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507626
Supporting Variants
Samples
Known GenesNOMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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