A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550699



Internal ID15991422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44372809..44386755hg38UCSC Ensembl
Innerchr10:44868257..44882203hg19UCSC Ensembl
Innerchr10:44188263..44202209hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813947
hg1913947
hg1813947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747327
Samples
Known GenesCXCL12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550699
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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