A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464219



Internal ID21121772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47700188..47707448hg38UCSC Ensembl
chr11:47721740..47729000hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387261
hg197261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991167
Samples
Known GenesAGBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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