A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053098



Internal ID18795629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12904089..12926547hg38UCSC Ensembl
Innerchr10:12946089..12968547hg19UCSC Ensembl
Innerchr10:12986095..13008553hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822459
hg1922459
hg1822459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521489
Samples
Known GenesCCDC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053098
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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