A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540453



Internal ID20913745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168162904..168164405hg38UCSC Ensembl
chr2:169019414..169020915hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4184n223
Supporting Variantsnssv18256255
Samples
Known GenesSTK39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540453
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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