A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551669



Internal ID16339078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81374678..82080786hg38UCSC Ensembl
Innerchr10:83134434..83840542hg19UCSC Ensembl
Innerchr10:83124414..83830522hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38706109
hg19706109
hg18706109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751932
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551669
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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