A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551540



Internal ID15992263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76494954..76500936hg38UCSC Ensembl
Innerchr10:78254712..78260694hg19UCSC Ensembl
Innerchr10:77924718..77930700hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385983
hg195983
hg185983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750307, nssv750308, nssv750309, nssv750310
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551540
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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