A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505007



Internal ID20878272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95159132..95161902hg38UCSC Ensembl
chr14:95625469..95628239hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382771
hg192771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022195
Samples
Known GenesDICER1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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