A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536291



Internal ID20909644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31846145..31847210hg38UCSC Ensembl
chr2:32071214..32072279hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536291
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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