A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466618



Internal ID21124171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97538909..97690647hg38UCSC Ensembl
chr11:97409909..97561647hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38151739
hg19151739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995804
Samples
Known GenesMIR7976
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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