A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056153



Internal ID19145372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47156912..47167354hg38UCSC Ensembl
Innerchr22:47552555..47562997hg19UCSC Ensembl
Innerchr22:45931219..45941661hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3810443
hg1910443
hg1810443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592269
Samples
Known GenesTBC1D22A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056153
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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