A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561507



Internal ID20934578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30133808..30134795hg38UCSC Ensembl
chr8:29991324..29992311hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277669
Samples
Known GenesLEPROTL1, MBOAT4, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561507
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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