A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057903



Internal ID18800434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15486426..15922838hg38UCSC Ensembl
Innerchr22:16055171..16491537hg19UCSC Ensembl
Innerchr22:14435171..14871537hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38436413
hg19436367
hg18436367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4453n100
Supporting Variantsnssv3589205, nssv3589204
Samples
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057903
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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