A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606340



Internal ID16047063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16868921..17295275hg38UCSC Ensembl
Innerchr7:16908545..17334899hg19UCSC Ensembl
Innerchr7:16875070..17301424hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38426355
hg19426355
hg18426355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11225n54
Supporting Variantsnssv1079629
Samples
Known GenesAGR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606340
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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