A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591701



Internal ID20964772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64314878..64315719hg38UCSC Ensembl
chr14:64781596..64782437hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237375
Samples
Known GenesESR2, MIR548AZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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