A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543369



Internal ID20916617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218914864..218915513hg38UCSC Ensembl
chr2:219779586..219780235hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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