A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595251



Internal ID20968322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88631391..88631654hg38UCSC Ensembl
chr14:89097735..89097998hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237598
Samples
Known GenesEML5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595251
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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