A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591698



Internal ID20964769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56641069..56642005hg38UCSC Ensembl
chr12:57034853..57035789hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38937
hg19937
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217627
Samples
Known GenesATP5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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