A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463044



Internal ID21120597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37930327..38067751hg38UCSC Ensembl
chr11:37951877..38089301hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38137425
hg19137425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463044
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