A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556579



Internal ID20929650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71969953..71970410hg38UCSC Ensembl
chr5:71265780..71266237hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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