A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562880



Internal ID20935951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140542654..140543686hg38UCSC Ensembl
chr5:139922239..139923271hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381033
hg191033
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5955n223
Supporting Variantsnssv18267494
Samples
Known GenesANKHD1-EIF4EBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562880
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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