A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592428



Internal ID20965499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51185976..51190096hg38UCSC Ensembl
chr12:51579759..51583879hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg384121
hg194121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219466
Samples
Known GenesPOU6F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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