A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007568



Internal ID19096787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68664858..68698250hg38UCSC Ensembl
Innerchr3:68714009..68747401hg19UCSC Ensembl
Innerchr3:68796699..68830091hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3833393
hg1933393
hg1833393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593979
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)nsv1007568
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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