A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557879



Internal ID20930950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104924030..104930941hg38UCSC Ensembl
chr4:105845187..105852098hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386912
hg196912
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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