A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576430



Internal ID20949501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15626627..15626943hg38UCSC Ensembl
chr12:15779561..15779877hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218367
Samples
Known GenesEPS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576430
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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