A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006478



Internal ID19095695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194517661..194548463hg38UCSC Ensembl
Innerchr3:194238390..194269192hg19UCSC Ensembl
Innerchr3:195719679..195750481hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3830803
hg1930803
hg1830803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611369
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)nsv1006478
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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