A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577311



Internal ID20950382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75773617..75774690hg38UCSC Ensembl
chr14:76239960..76241033hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237472
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577311
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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