A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577694



Internal ID20950765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74694776..74695305hg38UCSC Ensembl
chr14:75161479..75162008hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237273
Samples
Known GenesAREL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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