A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004136



Internal ID19093353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:116120853..116549678hg38UCSC Ensembl
Innerchr4:117042009..117470834hg19UCSC Ensembl
Innerchr4:117261458..117690282hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38428826
hg19428826
hg18428825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5370n100
Supporting Variantsnssv3743085
Samples
Known GenesMIR1973
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004136
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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