A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001807



Internal ID18744338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109232266..109318313hg38UCSC Ensembl
Innerchr3:108951113..109037160hg19UCSC Ensembl
Innerchr3:110433803..110519850hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3886048
hg1986048
hg1886048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3735251
Samples
Known GenesDPPA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001807
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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