A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594961



Internal ID20968032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2407765..2408173hg38UCSC Ensembl
chr16:2457766..2458174hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242700
Samples
Known GenesABCA17P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594961
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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