A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551682



Internal ID16339091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81874442..81875381hg38UCSC Ensembl
Innerchr10:83634198..83635137hg19UCSC Ensembl
Innerchr10:83624178..83625117hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38940
hg19940
hg18940
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751946, nssv751947, nssv751945, nssv751948
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551682
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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