A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558171



Internal ID20931242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57997380..58017724hg38UCSC Ensembl
chr5:57293207..57313551hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3820345
hg1920345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558171
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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