A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543237



Internal ID20916489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191510469..191511445hg38UCSC Ensembl
chr2:192375195..192376171hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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