A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018741



Internal ID20585781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45152082..45286978hg38UCSC Ensembl
chr14:45621285..45756181hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38134897
hg19134897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494098
Supporting Variants
Samples
Known GenesFANCM, MIS18BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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