A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576202



Internal ID20949273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91714638..91715275hg38UCSC Ensembl
chr14:92180982..92181619hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2236n223
Supporting Variantsnssv18237691
Samples
Known GenesCATSPERB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer