A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151635



Internal ID15529605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25254439..25514700hg38UCSC Ensembl
Innerchr22:25650406..25910667hg19UCSC Ensembl
Innerchr22:23980406..24240667hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38260262
hg19260262
hg18260262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588772
Supporting Variants
SamplesHGDP00815
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151635
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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