A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538992



Internal ID20912299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191048796..191049271hg38UCSC Ensembl
chr2:191913522..191913997hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4231n223
Supporting Variantsnssv18256994
Samples
Known GenesSTAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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