A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579254



Internal ID20952325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31465409..31466362hg38UCSC Ensembl
chr12:31618343..31619296hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217561
Samples
Known GenesDENND5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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