A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470180



Internal ID21127733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61982724..61993653hg38UCSC Ensembl
chr11:61750196..61761125hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3810930
hg1910930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470180
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