A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565940



Internal ID20939011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39690456..39691800hg38UCSC Ensembl
chr4:39692076..39693420hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565940
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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