A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508103



Internal ID20881401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92204469..92207622hg38UCSC Ensembl
chr14:92670813..92673966hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg383154
hg193154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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