A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551076



Internal ID20924216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109579570..109579844hg38UCSC Ensembl
chr2:110337147..110337421hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256471
Samples
Known GenesSEPT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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