A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028255



Internal ID20595295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10174128..10174693hg38UCSC Ensembl
chr16:10267985..10268550hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502482
Supporting Variants
Samples
Known GenesGRIN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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