A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564826



Internal ID20937897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121385551..121883506hg38UCSC Ensembl
chr5:120721246..121219201hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38497956
hg19497956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266197
Samples
Known GenesFTMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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