A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557829



Internal ID20930900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6350681..6355845hg38UCSC Ensembl
chr5:6350794..6355958hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385165
hg195165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557829
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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