A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032666



Internal ID18775200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170481074..170631706hg38UCSC Ensembl
Innerchr4:171402225..171552857hg19UCSC Ensembl
Innerchr4:171638800..171789432hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38150633
hg19150633
hg18150633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744512
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032666
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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