A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903827



Internal ID22678998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116429650..116429968hg38UCSC Ensembl
chr6:116750813..116751131hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423131
Samples
Known GenesDSE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903827
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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