A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029517



Internal ID19118736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186931664..187177808hg38UCSC Ensembl
Innerchr4:187852818..188098962hg19UCSC Ensembl
Innerchr4:188089812..188335956hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38246145
hg19246145
hg18246145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635641
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)nsv1029517
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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