A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033902



Internal ID18776436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143193260..143364619hg38UCSC Ensembl
Innerchr4:144114413..144285772hg19UCSC Ensembl
Innerchr4:144333863..144505222hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38171360
hg19171360
hg18171360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641195
Samples
Known GenesGAB1, MIR3139, USP38
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033902
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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