A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595364



Internal ID20968435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30512297..30513007hg38UCSC Ensembl
chr16:30523618..30524328hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243505
Samples
Known GenesITGAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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