A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584661



Internal ID20957732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:23577438..23577851hg38UCSC Ensembl
chr12:23730372..23730785hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1444n223
Supporting Variantsnssv18226474
Samples
Known GenesSOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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