A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570163



Internal ID20943234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67135423..67136353hg38UCSC Ensembl
chr8:68047658..68048588hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278537
Samples
Known GenesCSPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570163
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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