A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488774



Internal ID21146327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80176622..80177530hg38UCSC Ensembl
chr14:80642965..80643873hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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