A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027518



Internal ID18770050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188895421..189857367hg38UCSC Ensembl
Innerchr4:189816575..190778522hg19UCSC Ensembl
Innerchr4:190053569..191015516hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38961947
hg19961948
hg18961948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636445
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)nsv1027518
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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