A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590142



Internal ID20963213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9267620..9594861hg38UCSC Ensembl
chr16:9361477..9688718hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38327242
hg19327242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240939
Samples
Known GenesMIR7641-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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