A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559256



Internal ID20932327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74600232..74600719hg38UCSC Ensembl
chr8:75512467..75512954hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278710
Samples
Known GenesFLJ39080
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559256
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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