A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012536



Internal ID19101753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3899113..4174890hg38UCSC Ensembl
Innerchr4:3900840..4176617hg19UCSC Ensembl
Innerchr4:3870638..4227518hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38275778
hg19275778
hg18356881
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5087n100
Supporting Variantsnssv3738127, nssv3616144
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)nsv1012536
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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