A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016739



Internal ID18759274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186328740..186613274hg38UCSC Ensembl
Innerchr4:187249894..187534428hg19UCSC Ensembl
Innerchr4:187486888..187771422hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38284535
hg19284535
hg18284535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5494n100
Supporting Variantsnssv3635633
Samples
Known GenesF11-AS1, FAT1, MTNR1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016739
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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