A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501777



Internal ID20875014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11475113..11716333hg38UCSC Ensembl
chr16:11568969..11810189hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38241221
hg19241221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192154
Samples
Known GenesLITAF, SNN, TXNDC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501777
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer