A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551879



Internal ID15992602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90322493..90800151hg38UCSC Ensembl
Innerchr10:92082250..92559908hg19UCSC Ensembl
Innerchr10:92072230..92549888hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38477659
hg19477659
hg18477659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1338n54
Supporting Variantsnssv1174265
SamplesNINDS_59
Known GenesHTR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551879
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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