A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463995



Internal ID21121548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118530301..118531000hg38UCSC Ensembl
chr11:118401016..118401715hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987194
Samples
Known GenesTTC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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