A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014738



Internal ID19103955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18752404..18785389hg38UCSC Ensembl
Innerchr4:18754027..18787012hg19UCSC Ensembl
Innerchr4:18363125..18396110hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3832986
hg1932986
hg1832986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737704
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014738
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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