A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476123



Internal ID21133676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73881717..73882804hg38UCSC Ensembl
chr14:74348420..74349507hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021430
Samples
Known GenesPTGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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