A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581031



Internal ID20954102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45436732..45437859hg38UCSC Ensembl
chr12:45830515..45831642hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230208
Samples
Known GenesANO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581031
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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