A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477112



Internal ID21134665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31365065..31365722hg38UCSC Ensembl
chr14:31834271..31834928hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017757
Samples
Known GenesHEATR5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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