A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591260



Internal ID20964331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98596965..98597465hg38UCSC Ensembl
chr12:98990743..98991243hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229236
Samples
Known GenesSLC25A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591260
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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