A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468007



Internal ID21125560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102338576..102345082hg38UCSC Ensembl
chr11:102209307..102215813hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg386507
hg196507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985469
Samples
Known GenesBIRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468007
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