A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061257



Internal ID18803788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21212930..21563022hg38UCSC Ensembl
Innerchr22:21567219..21917311hg19UCSC Ensembl
Innerchr22:19897219..20247311hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38350093
hg19350093
hg18350093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4488n100
Supporting Variantsnssv3587508, nssv3587503, nssv3731883, nssv3587505, nssv3587504, nssv3587507, nssv3587506
Samples
Known GenesHIC2, PI4KAP2, POM121L8P, RIMBP3B, RIMBP3C, TMEM191C, UBE2L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061257
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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