A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471950



Internal ID21129503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122130563..122131666hg38UCSC Ensembl
chr11:122001271..122002374hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987618
Samples
Known GenesMIR100HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471950
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