A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586529



Internal ID20959600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26032017..26035234hg38UCSC Ensembl
chr12:26184950..26188167hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg383218
hg193218
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224906
Samples
Known GenesRASSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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