A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016493



Internal ID20583533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101043380..101044695hg38UCSC Ensembl
chr14:101509717..101511032hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499824
Supporting Variants
Samples
Known GenesMIR1185-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016493
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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