A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066760



Internal ID19155979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48767465..48783199hg38UCSC Ensembl
Innerchr22:49163277..49179011hg19UCSC Ensembl
Innerchr22:47549283..47565017hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3815735
hg1915735
hg1815735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4589n100
Supporting Variantsnssv3592289
Samples
Known GenesMIR4535
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066760
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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