A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540289



Internal ID20913579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79035679..79038070hg38UCSC Ensembl
chr2:79262805..79265196hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg382392
hg192392
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540289
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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