A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551559



Internal ID15992282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78264044..78290492hg38UCSC Ensembl
Innerchr10:80023801..80050249hg19UCSC Ensembl
Innerchr10:79693807..79720255hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3826449
hg1926449
hg1826449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1273n54
Supporting Variantsnssv751741
Samples
Known GenesLINC00595
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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