A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585280



Internal ID20958351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25842207..25842918hg38UCSC Ensembl
chr12:25995141..25995852hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585280
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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