A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540488



Internal ID20913780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46638282..46639251hg38UCSC Ensembl
chr2:46865421..46866390hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38970
hg19970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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