A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896832



Internal ID22671928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8932738..9162828hg38UCSC Ensembl
chr6:8932971..9163061hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38230091
hg19230091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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