A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551910



Internal ID16339319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90857538..90858273hg38UCSC Ensembl
Innerchr10:92617295..92618030hg19UCSC Ensembl
Innerchr10:92607275..92608010hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38736
hg19736
hg18736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1346n54
Supporting Variantsnssv753447, nssv753446
Samples
Known GenesHTR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551910
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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