A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576864



Internal ID20949935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57767915..57768192hg38UCSC Ensembl
chr16:57801827..57802104hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239324
Samples
Known GenesKIFC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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