A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263715



Internal ID20830755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127689148..127689550hg38UCSC Ensembl
chr4:128610303..128610705hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566698
Supporting Variants
Samples
Known GenesINTU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263715
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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