A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437683



Internal ID21095236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3395168..3594274hg38UCSC Ensembl
chr11:3416398..3615504hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38199107
hg19199107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990815
Samples
Known GenesLOC650368
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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