A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540162



Internal ID20913454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24071002..24071544hg38UCSC Ensembl
chr2:24293872..24294414hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257482
Samples
Known GenesSF3B14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540162
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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