A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277292



Internal ID20844332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14287468..14289691hg38UCSC Ensembl
chr8:14144977..14147200hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382224
hg192224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562175
Supporting Variants
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277292
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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