A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473761



Internal ID21131314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95371605..95372377hg38UCSC Ensembl
chr11:95104769..95105541hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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