A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512955



Internal ID20886295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103571933..103579692hg38UCSC Ensembl
chr14:104038270..104046029hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg387760
hg197760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015925
Samples
Known GenesAPOPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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