A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551479



Internal ID15992202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70007598..70179618hg38UCSC Ensembl
Innerchr10:71767354..71939374hg19UCSC Ensembl
Innerchr10:71437360..71609380hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38172021
hg19172021
hg18172021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750122
Samples
Known GenesAIFM2, H2AFY2, SAR1A, TYSND1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551479
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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