A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550487



Internal ID20923628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30132537..30133330hg38UCSC Ensembl
chr2:30355403..30356196hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550487
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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