A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020315



Internal ID20587355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60808531..60817760hg38UCSC Ensembl
chr14:61275249..61284478hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg389230
hg199230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492346
Supporting Variants
Samples
Known GenesMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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