A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941901



Internal ID22717332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21203874..21208224hg38UCSC Ensembl
chr17:21107187..21111537hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384351
hg194351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383205
Samples
Known GenesTMEM11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941901
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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