A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041297



Internal ID18783828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43055119..43095609hg38UCSC Ensembl
Innerchr10:43550567..43591057hg19UCSC Ensembl
Innerchr10:42870573..42911063hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3840491
hg1940491
hg1840491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv723n100
Supporting Variantsnssv3511079
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)nsv1041297
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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