A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034242



Internal ID19123464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170316812..170368212hg38UCSC Ensembl
Innerchr4:171237963..171289363hg19UCSC Ensembl
Innerchr4:171474538..171525938hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3851401
hg1951401
hg1851401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635383
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)nsv1034242
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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