A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587092



Internal ID20960163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48674183..48674875hg38UCSC Ensembl
chr12:49067966..49068658hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223020
Samples
Known GenesKANSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587092
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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