A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016572



Internal ID20583612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20785698..20787005hg38UCSC Ensembl
chr14:21253857..21255164hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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