A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606629



Internal ID16047352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38248669..38302014hg38UCSC Ensembl
Innerchr7:38288270..38341615hg19UCSC Ensembl
Innerchr7:38254795..38308140hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3853346
hg1953346
hg1853346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11275n54
Supporting Variantsnssv1082716, nssv1082715
Samples
Known GenesTARP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606629
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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