A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045283



Internal ID19134502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..113464hg38UCSC Ensembl
Innerchr10:72797..159404hg19UCSC Ensembl
Innerchr10:62797..149404hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3886604
hg1986608
hg1886608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n100
Supporting Variantsnssv3489528
Samples
Known GenesTUBB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045283
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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