A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549863



Internal ID16337272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4662517..4668049hg38UCSC Ensembl
Innerchr10:4704709..4710241hg19UCSC Ensembl
Innerchr10:4694709..4700241hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385533
hg195533
hg185533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv742173
Samples
Known GenesLINC00704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549863
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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