A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606189



Internal ID16393598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10497229..10578162hg38UCSC Ensembl
Innerchr7:10536856..10617789hg19UCSC Ensembl
Innerchr7:10503381..10584314hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3880934
hg1980934
hg1880934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11201n54
Supporting Variantsnssv1079134
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606189
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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