A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277920



Internal ID20844960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38334493..38335163hg38UCSC Ensembl
chr8:38192011..38192681hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571689
Supporting Variants
Samples
Known GenesWHSC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277920
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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