A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539136



Internal ID20912443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12709911..12711091hg38UCSC Ensembl
chr2:12850037..12851217hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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