A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056768



Internal ID18799299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20044066..20077847hg38UCSC Ensembl
Innerchr22:20031589..20065370hg19UCSC Ensembl
Innerchr22:18411589..18445370hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3833782
hg1933782
hg1833782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3587358
Samples
Known GenesTANGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056768
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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