A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590860



Internal ID20963931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100399071..100399790hg38UCSC Ensembl
chr12:100792849..100793568hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220047
Samples
Known GenesSLC17A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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