A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570855



Internal ID20943926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:3650292..5275479hg38UCSC Ensembl
chr8:3507814..5133001hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg381625188
hg191625188
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277862
Samples
Known GenesCSMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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