A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002080



Internal ID18744611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109315528..109412007hg38UCSC Ensembl
Innerchr3:109034375..109130854hg19UCSC Ensembl
Innerchr3:110517065..110613544hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3896480
hg1996480
hg1896480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604404
Samples
Known GenesDPPA2, DPPA4, FLJ25363
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002080
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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