A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592856



Internal ID20965927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7738923..7870946hg38UCSC Ensembl
chr16:7788925..7920948hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38132024
hg19132024
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592856
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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