A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539118



Internal ID20912425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170909185..170909870hg38UCSC Ensembl
chr2:171765695..171766380hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539118
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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