A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575848



Internal ID20948919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56730461..56730812hg38UCSC Ensembl
chr12:57124245..57124596hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219109
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575848
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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