A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005284



Internal ID18747815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8778715..8816515hg38UCSC Ensembl
Innerchr3:8820401..8858201hg19UCSC Ensembl
Innerchr3:8795401..8833201hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837801
hg1937801
hg1837801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4678n100
Supporting Variantsnssv3739589, nssv3591856, nssv3739590
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)nsv1005284
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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