A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571718



Internal ID20944789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140542918..140543834hg38UCSC Ensembl
chr5:139922503..139923419hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5955n223
Supporting Variantsnssv18267495
Samples
Known GenesANKHD1-EIF4EBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571718
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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