A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539061



Internal ID20912368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32553062..32553430hg38UCSC Ensembl
chr2:32778129..32778497hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260089
Samples
Known GenesBIRC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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