A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606159



Internal ID16393568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9478892..9532468hg38UCSC Ensembl
Innerchr7:9518522..9572098hg19UCSC Ensembl
Innerchr7:9485047..9538623hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3853577
hg1953577
hg1853577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079118
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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