A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550398



Internal ID15991121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34885707..35271661hg38UCSC Ensembl
Innerchr10:35174635..35560589hg19UCSC Ensembl
Innerchr10:35214641..35600595hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38385955
hg19385955
hg18385955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv746837
Samples
Known GenesCCNY, CREM, CUL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550398
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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