A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060635



Internal ID18803166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15327990..15617982hg38UCSC Ensembl
Innerchr22:16359981..16649973hg19UCSC Ensembl
Innerchr22:14739981..15029973hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38289993
hg19289993
hg18289993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589269
Samples
Known GenesOR11H1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060635
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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