A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569696



Internal ID20942767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36551671..36552366hg38UCSC Ensembl
chr5:36551773..36552468hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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