A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582492



Internal ID20955563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76396565..76396955hg38UCSC Ensembl
chr12:76790345..76790735hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1618n223
Supporting Variantsnssv18225588
Samples
Known GenesOSBPL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582492
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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