A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001255



Internal ID19090472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:116120853..116573353hg38UCSC Ensembl
Innerchr4:117042009..117494509hg19UCSC Ensembl
Innerchr4:117261458..117713957hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38452501
hg19452501
hg18452500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5370n100
Supporting Variantsnssv3639332
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)nsv1001255
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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