A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014636



Internal ID19103854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:78415545..78442260hg38UCSC Ensembl
Innerchr3:78464695..78491410hg19UCSC Ensembl
Innerchr3:78547385..78574100hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3826716
hg1926716
hg1826716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596216, nssv3596215
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)nsv1014636
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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