A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006007



Internal ID19095225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68402059..68425211hg38UCSC Ensembl
Innerchr3:68451209..68474361hg19UCSC Ensembl
Innerchr3:68533899..68557051hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3823153
hg1923153
hg1823153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4770n100
Supporting Variantsnssv3593974
Samples
Known GenesFAM19A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006007
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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