A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461682



Internal ID21119235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72012812..72019522hg38UCSC Ensembl
chr11:71723858..71730568hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386711
hg196711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992762
Samples
Known GenesLOC100128494, NUMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461682
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