A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061384



Internal ID19150603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:32769478..32795825hg38UCSC Ensembl
Innerchr22:33165464..33191811hg19UCSC Ensembl
Innerchr22:31495464..31521811hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3826348
hg1926348
hg1826348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600823
Samples
Known GenesSYN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061384
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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