A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276122



Internal ID20843162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123399964..123418938hg38UCSC Ensembl
chr8:124412204..124431178hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3818975
hg1918975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556771
Supporting Variants
Samples
Known GenesWDYHV1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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