A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577561



Internal ID20950632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74721291..74721527hg38UCSC Ensembl
chr14:75187994..75188230hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237274
Samples
Known GenesFCF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577561
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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