A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551521



Internal ID15992244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73873872..73874574hg38UCSC Ensembl
Innerchr10:75633630..75634332hg19UCSC Ensembl
Innerchr10:75303636..75304338hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38703
hg19703
hg18703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750279
Samples
Known GenesCAMK2G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551521
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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