A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562325



Internal ID20935396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44554537..44554622hg38UCSC Ensembl
chr5:44554639..44554724hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268411
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562325
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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