A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491564



Internal ID21149117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73857179..73861177hg38UCSC Ensembl
chr14:74323882..74327880hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg383999
hg193999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021429
Samples
Known GenesPTGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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