A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013710



Internal ID18756242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4174890hg38UCSC Ensembl
Innerchr4:3885796..4176617hg19UCSC Ensembl
Innerchr4:3855594..4227518hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38290822
hg19290822
hg18371925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5085n100
Supporting Variantsnssv3738111, nssv3738112, nssv3738113
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013710
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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