A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001848



Internal ID19091065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3912156..4173838hg38UCSC Ensembl
Innerchr4:3913883..4175565hg19UCSC Ensembl
Innerchr4:3964803..4226466hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38261683
hg19261683
hg18261664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5089n100
Supporting Variantsnssv3616161
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)nsv1001848
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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