A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592527



Internal ID20965598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92902461..92903189hg38UCSC Ensembl
chr12:93296237..93296965hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1652n223
Supporting Variantsnssv18234408
Samples
Known GenesEEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592527
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer