A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549281



Internal ID20922449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168162876..168164498hg38UCSC Ensembl
chr2:169019386..169021008hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381623
hg191623
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4184n223
Supporting Variantsnssv18256254
Samples
Known GenesSTK39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549281
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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