A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571387



Internal ID20944458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156836552..156838131hg38UCSC Ensembl
chr5:156263563..156265142hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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