A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048232



Internal ID18790763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..228735hg38UCSC Ensembl
Innerchr10:72797..274675hg19UCSC Ensembl
Innerchr10:62797..264675hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38201875
hg19201879
hg18201879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv649n100
Supporting Variantsnssv3502241, nssv3501067
Samples
Known GenesTUBB8, ZMYND11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048232
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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