A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551880



Internal ID15992603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90323258..90838701hg38UCSC Ensembl
Innerchr10:92083015..92598458hg19UCSC Ensembl
Innerchr10:92072995..92588438hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38515444
hg19515444
hg18515444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1338n54
Supporting Variantsnssv753330
Samples
Known GenesHTR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551880
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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