A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050957



Internal ID18793488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43083220..43095955hg38UCSC Ensembl
Innerchr10:43578668..43591403hg19UCSC Ensembl
Innerchr10:42898674..42911409hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3812736
hg1912736
hg1812736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv727n100
Supporting Variantsnssv3517502
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)nsv1050957
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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