A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551542



Internal ID15992265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76496115..76498584hg38UCSC Ensembl
Innerchr10:78255873..78258342hg19UCSC Ensembl
Innerchr10:77925879..77928348hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382470
hg192470
hg182470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750312
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551542
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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