A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571658



Internal ID20944729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1512326..1512686hg38UCSC Ensembl
chr5:1512441..1512801hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268710
Samples
Known GenesLPCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571658
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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