A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047815



Internal ID18790346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118004235..118069532hg38UCSC Ensembl
Innerchr10:119763746..119829043hg19UCSC Ensembl
Innerchr10:119753736..119819033hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3865298
hg1965298
hg1865298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514330
Samples
Known GenesCASC2, RAB11FIP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047815
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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