A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551678



Internal ID16339087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81874391..81875381hg38UCSC Ensembl
Innerchr10:83634147..83635137hg19UCSC Ensembl
Innerchr10:83624127..83625117hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38991
hg19991
hg18991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1300n54
Supporting Variantsnssv751940, nssv751939
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551678
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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