A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606675



Internal ID16394084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39503235..39510748hg38UCSC Ensembl
Innerchr7:39542834..39550347hg19UCSC Ensembl
Innerchr7:39509359..39516872hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg387514
hg197514
hg187514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11283n54
Supporting Variantsnssv1082842
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606675
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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