A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515501



Internal ID20888861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91931334..91932437hg38UCSC Ensembl
chr14:92397678..92398781hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021798
Samples
Known GenesFBLN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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