A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558802



Internal ID20931873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12947671..12948297hg38UCSC Ensembl
chr4:12949295..12949921hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263030
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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