A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013487



Internal ID18756018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9970387..10319339hg38UCSC Ensembl
Innerchr4:9972011..10320963hg19UCSC Ensembl
Innerchr4:9581109..9930061hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38348953
hg19348953
hg18348953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613423
Samples
Known GenesMIR3138, SLC2A9, WDR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013487
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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