A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579721



Internal ID20952792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112038103..112039038hg38UCSC Ensembl
chr12:112475907..112476842hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227706
Samples
Known GenesNAA25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579721
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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