A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055708



Internal ID19144927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39264031..39294305hg38UCSC Ensembl
Innerchr22:39660036..39690310hg19UCSC Ensembl
Innerchr22:37989982..38020256hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3830275
hg1930275
hg1830275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590786
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055708
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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