A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050135



Internal ID19139354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..97603hg38UCSC Ensembl
Innerchr10:72797..143543hg19UCSC Ensembl
Innerchr10:62797..133543hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3870743
hg1970747
hg1870747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n100
Supporting Variantsnssv3502158, nssv3498026, nssv3491661, nssv3499503, nssv3500391, nssv3494402
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)nsv1050135
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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