A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590147



Internal ID20963218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13774086..13774747hg38UCSC Ensembl
chr16:13867943..13868604hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590147
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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