A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585564



Internal ID20958635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25229987..25230637hg38UCSC Ensembl
chr12:25382921..25383571hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224426
Samples
Known GenesKRAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585564
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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