A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058551



Internal ID19147770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25392467..25522742hg38UCSC Ensembl
Innerchr22:25788434..25918709hg19UCSC Ensembl
Innerchr22:24118434..24248709hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38130276
hg19130276
hg18130276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4558n100
Supporting Variantsnssv3600777
Samples
Known GenesCRYBB2P1, MIR6817
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058551
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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