A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008133



Internal ID19097352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28868819..28908556hg38UCSC Ensembl
Innerchr3:28910310..28950047hg19UCSC Ensembl
Innerchr3:28885314..28925051hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3839738
hg1939738
hg1839738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589570
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)nsv1008133
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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