A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888587



Internal ID22663595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50570130..50580575hg38UCSC Ensembl
chr6:50537843..50548288hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3810446
hg1910446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888587
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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