A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561590



Internal ID20934661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30099321..30100463hg38UCSC Ensembl
chr8:29956837..29957979hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277667
Samples
Known GenesLEPROTL1, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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