A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006449



Internal ID19095666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16336568..16410921hg38UCSC Ensembl
Innerchr4:16338191..16412544hg19UCSC Ensembl
Innerchr4:15947289..16021642hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3874354
hg1974354
hg1874354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619858
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)nsv1006449
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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