A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170004



Internal ID21314065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34003443..34013910hg38UCSC Ensembl
Outerchr22:34002196..34018477hg38UCSC Ensembl
Innerchr22:34399432..34409899hg19UCSC Ensembl
Outerchr22:34398185..34414466hg19UCSC Ensembl
Innerchr22:32729432..32739899hg18UCSC Ensembl
Outerchr22:32728185..32744466hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3816282
hg1916282
hg1816282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249117
SamplesMLY_13
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170004
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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