A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539279



Internal ID20912580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46890936..46891641hg38UCSC Ensembl
chr2:47118075..47118780hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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