A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594989



Internal ID20968060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45482706..45483389hg38UCSC Ensembl
chr12:45876489..45877172hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1532n223
Supporting Variantsnssv18223607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594989
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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