A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577825



Internal ID20950896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:99101838..99102465hg38UCSC Ensembl
chr12:99495616..99496243hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223268
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577825
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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