A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054078



Internal ID18796609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43083220..43096169hg38UCSC Ensembl
Innerchr10:43578668..43591617hg19UCSC Ensembl
Innerchr10:42898674..42911623hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3812950
hg1912950
hg1812950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv727n100
Supporting Variantsnssv3507617, nssv3512185, nssv3512772, nssv3519534, nssv3514902, nssv3504881, nssv3514187, nssv3504470, nssv3519523, nssv3506940, nssv3517377, nssv3519047, nssv3516568, nssv3513256
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)nsv1054078
Frequency
Sample Size29084
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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