A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474214



Internal ID21131767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89168270..89168899hg38UCSC Ensembl
chr11:88901438..88902067hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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