A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576512



Internal ID20949583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58734751..58735808hg38UCSC Ensembl
chr16:58768655..58769712hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576512
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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