A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594982



Internal ID20968053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31028467..31028690hg38UCSC Ensembl
chr14:31497673..31497896hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227810
Samples
Known GenesAP4S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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