A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606190



Internal ID16393599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10514333..10589304hg38UCSC Ensembl
Innerchr7:10553960..10628931hg19UCSC Ensembl
Innerchr7:10520485..10595456hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3874972
hg1974972
hg1874972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11201n54
Supporting Variantsnssv1079135
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606190
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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