A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011903



Internal ID19101121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11883204..11930919hg38UCSC Ensembl
Innerchr3:11924678..11972393hg19UCSC Ensembl
Innerchr3:11899678..11947393hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3847716
hg1947716
hg1847716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4683n100
Supporting Variantsnssv3591951
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)nsv1011903
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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