A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571523



Internal ID20944594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88480953..88481289hg38UCSC Ensembl
chr8:89493182..89493518hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571523
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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