A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890529



Internal ID22665557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117705082..117705151hg38UCSC Ensembl
chr6:118026245..118026314hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417743
Samples
Known GenesNUS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890529
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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