A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557495



Internal ID20930566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43680999..43681680hg38UCSC Ensembl
chr5:43681101..43681782hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268403
Samples
Known GenesNNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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