A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013938



Internal ID19103157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4180263hg38UCSC Ensembl
Innerchr4:3885796..4181990hg19UCSC Ensembl
Innerchr4:3855594..4232891hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38296195
hg19296195
hg18377298
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5087n100
Supporting Variantsnssv3616136, nssv3738114
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)nsv1013938
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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