A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016806



Internal ID20583846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25773602..25781197hg38UCSC Ensembl
chr14:26242808..26250403hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg387596
hg197596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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