A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609115



Internal ID16396524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154881129..154909643hg38UCSC Ensembl
Innerchr7:154672839..154701353hg19UCSC Ensembl
Innerchr7:154303772..154332286hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3828515
hg1928515
hg1828515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11742n54
Supporting Variantsnssv1100254
Samples
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609115
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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