A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557657



Internal ID20930728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166844882..166845396hg38UCSC Ensembl
chr5:166271887..166272401hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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