A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594075



Internal ID20967146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76555967..76823704hg38UCSC Ensembl
chr14:77022310..77290047hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38267738
hg19267738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237492
Samples
Known GenesANGEL1, LOC100506603, VASH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594075
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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