A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539623



Internal ID20912919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:204159185..204160396hg38UCSC Ensembl
chr2:205023908..205025119hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539623
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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