A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551681



Internal ID16339090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81874442..81875329hg38UCSC Ensembl
Innerchr10:83634198..83635085hg19UCSC Ensembl
Innerchr10:83624178..83625065hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38888
hg19888
hg18888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1300n54
Supporting Variantsnssv751943, nssv751944
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551681
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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