A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581421



Internal ID20954492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11785100..11785643hg38UCSC Ensembl
chr16:11878956..11879499hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239845
Samples
Known GenesZC3H7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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