A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038032



Internal ID18780563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73214302..73255397hg38UCSC Ensembl
Innerchr11:72925347..72966442hg19UCSC Ensembl
Innerchr11:72602995..72644090hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3841096
hg1941096
hg1841096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504533
Samples
Known GenesP2RY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038032
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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