A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606630



Internal ID16047353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38248669..38317722hg38UCSC Ensembl
Innerchr7:38288270..38357323hg19UCSC Ensembl
Innerchr7:38254795..38323848hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3869054
hg1969054
hg1869054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11274n54
Supporting Variantsnssv1082717
Samples
Known GenesTARP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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