A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556345



Internal ID20929416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154582517..154583277hg38UCSC Ensembl
chr5:153962077..153962837hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5992n223
Supporting Variantsnssv18268751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556345
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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