A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571065



Internal ID20944136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30135063..30135902hg38UCSC Ensembl
chr8:29992579..29993418hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277670
Samples
Known GenesLEPROTL1, MBOAT4, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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