A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904010



Internal ID22679183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109403631..109403828hg38UCSC Ensembl
chr6:109724834..109725031hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412649
Samples
Known GenesPPIL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904010
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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