A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579679



Internal ID20952750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71139012..71139975hg38UCSC Ensembl
chr12:71532792..71533755hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219580
Samples
Known GenesTSPAN8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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