A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579247



Internal ID20952318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25249374..25249997hg38UCSC Ensembl
chr16:25260695..25261318hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242756
Samples
Known GenesZKSCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579247
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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