A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580817



Internal ID20953888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110324611..110325507hg38UCSC Ensembl
chr12:110762416..110763312hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235308
Samples
Known GenesATP2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580817
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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