A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577781



Internal ID20950852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39411890..39412679hg38UCSC Ensembl
chr12:39805692..39806481hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234129
Samples
Known GenesKIF21A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577781
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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