A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278100



Internal ID20845140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47319822..52044550hg38UCSC Ensembl
chr8:48232411..52957110hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg384724729
hg194724700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569657
Supporting Variants
Samples
Known GenesC8orf22, CEBPD, EFCAB1, LOC101929217, LOC101929268, MCM4, PCMTD1, PRKDC, PXDNL, SNAI2, SNTG1, SPIDR, UBE2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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