A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014108



Internal ID19103328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103226498..103269840hg38UCSC Ensembl
Innerchr3:102945342..102988684hg19UCSC Ensembl
Innerchr3:104428032..104471374hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3843343
hg1943343
hg1843343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604378
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)nsv1014108
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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