A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015916



Internal ID19105134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133323922..133385035hg38UCSC Ensembl
Innerchr4:134245077..134306190hg19UCSC Ensembl
Innerchr4:134464527..134525640hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3861114
hg1961114
hg1861114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639529
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)nsv1015916
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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