A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550202



Internal ID16337611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21567546..21738715hg38UCSC Ensembl
Innerchr10:21856475..22027644hg19UCSC Ensembl
Innerchr10:21896481..22067650hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38171170
hg19171170
hg18171170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744703
Samples
Known GenesMLLT10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550202
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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