A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031421



Internal ID20598461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74567312..74568702hg38UCSC Ensembl
chr16:74601210..74602600hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514981
Supporting Variants
Samples
Known GenesGLG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00093


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