A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012039



Internal ID19101257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6135592..6208735hg38UCSC Ensembl
Innerchr3:6177279..6250422hg19UCSC Ensembl
Innerchr3:6152279..6225422hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3873144
hg1973144
hg1873144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739584
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)nsv1012039
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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