A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277761



Internal ID20844801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32479238..32479684hg38UCSC Ensembl
chr8:32336754..32337200hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556372
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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