A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499057



Internal ID20872273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97419205..97423511hg38UCSC Ensembl
chr14:97885542..97889848hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384307
hg194307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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