A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056922



Internal ID19146141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25293094..25515469hg38UCSC Ensembl
Innerchr22:25689061..25911436hg19UCSC Ensembl
Innerchr22:24019061..24241436hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38222376
hg19222376
hg18222376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4547n100
Supporting Variantsnssv3600577, nssv3600575, nssv3600576
Samples
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056922
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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