A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460333



Internal ID21117886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62522521..62524878hg38UCSC Ensembl
chr11:62289993..62292350hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382358
hg192358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993211
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460333
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