A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012880



Internal ID19102097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180054495..180117775hg38UCSC Ensembl
Innerchr3:179772283..179835563hg19UCSC Ensembl
Innerchr3:181254977..181318257hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3863281
hg1963281
hg1863281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614998
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)nsv1012880
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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