A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610717



Internal ID16051440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18327655..18400806hg38UCSC Ensembl
Innerchr8:18185164..18258316hg19UCSC Ensembl
Innerchr8:18229444..18302596hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3873152
hg1973153
hg1873153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107412
Samples
Known GenesNAT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610717
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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