A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551911



Internal ID16339320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90857538..90858325hg38UCSC Ensembl
Innerchr10:92617295..92618082hg19UCSC Ensembl
Innerchr10:92607275..92608062hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38788
hg19788
hg18788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1346n54
Supporting Variantsnssv753448, nssv753449
Samples
Known GenesHTR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551911
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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