A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551670



Internal ID16339079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81545860..81972366hg38UCSC Ensembl
Innerchr10:83305616..83732122hg19UCSC Ensembl
Innerchr10:83295596..83722102hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38426507
hg19426507
hg18426507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751933
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551670
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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