A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563190



Internal ID20936261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44815590..44816234hg38UCSC Ensembl
chr5:44815692..44816336hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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