A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561917



Internal ID20934988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137449634..137458770hg38UCSC Ensembl
chr8:138461877..138471013hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg389137
hg199137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561917
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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