A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563689



Internal ID20936760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68043737..68044815hg38UCSC Ensembl
chr5:67339565..67340643hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5783n223
Supporting Variantsnssv18266961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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