A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052444



Internal ID18794975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43083220..43096671hg38UCSC Ensembl
Innerchr10:43578668..43592119hg19UCSC Ensembl
Innerchr10:42898674..42912125hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813452
hg1913452
hg1813452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv727n100
Supporting Variantsnssv3522525, nssv3506513
Samples
Known GenesRET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052444
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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