A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587339



Internal ID20960410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61742684..61743283hg38UCSC Ensembl
chr14:62209402..62210001hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237182
Samples
Known GenesHIF1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587339
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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