A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548270



Internal ID20921462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62428729..62429289hg38UCSC Ensembl
chr2:62655864..62656424hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548270
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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