A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549880



Internal ID16337289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4738837..4768369hg38UCSC Ensembl
Innerchr10:4781029..4810561hg19UCSC Ensembl
Innerchr10:4771029..4800561hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3829533
hg1929533
hg1829533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743469
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549880
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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