A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492931



Internal ID21150484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66729152..66732927hg38UCSC Ensembl
chr14:67195870..67199645hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg383776
hg193776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019976
Samples
Known GenesGPHN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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