A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592650



Internal ID20965721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14851835..14852545hg38UCSC Ensembl
chr12:15004769..15005479hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592650
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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