A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012312



Internal ID19101530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11883204..11910282hg38UCSC Ensembl
Innerchr3:11924678..11951756hg19UCSC Ensembl
Innerchr3:11899678..11926756hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3827079
hg1927079
hg1827079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591943
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)nsv1012312
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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