A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578785



Internal ID20951856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31047388..31049201hg38UCSC Ensembl
chr14:31516594..31518407hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381814
hg191814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220471
Samples
Known GenesAP4S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578785
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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