A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033326



Internal ID19122548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170512663..170546379hg38UCSC Ensembl
Innerchr4:171433814..171467530hg19UCSC Ensembl
Innerchr4:171670389..171704105hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3833717
hg1933717
hg1833717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635391
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)nsv1033326
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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