A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054622



Internal ID19143841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..98151hg38UCSC Ensembl
Innerchr10:72797..144091hg19UCSC Ensembl
Innerchr10:62797..134091hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3871291
hg1971295
hg1871295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n100
Supporting Variantsnssv3494067, nssv3495985, nssv3500593
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)nsv1054622
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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