A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552969



Internal ID20926087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68461376..68461998hg38UCSC Ensembl
chr2:68688508..68689130hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552969
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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