A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558096



Internal ID20931167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166637976..166678971hg38UCSC Ensembl
chr4:167559127..167600122hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3840996
hg1940996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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