A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551732



Internal ID16339141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82471160..82520193hg38UCSC Ensembl
Innerchr10:84230916..84279949hg19UCSC Ensembl
Innerchr10:84220896..84269929hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3849034
hg1949034
hg1849034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752118
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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