A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033744



Internal ID19122965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144382482..144415800hg38UCSC Ensembl
Innerchr4:145303634..145336952hg19UCSC Ensembl
Innerchr4:145523084..145556402hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3833319
hg1933319
hg1833319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636062
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)nsv1033744
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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