A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000614



Internal ID19089831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:43916653..43970460hg38UCSC Ensembl
Innerchr3:43958145..44011952hg19UCSC Ensembl
Innerchr3:43933149..43986956hg18UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3853808
hg1953808
hg1853808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589733, nssv3589734
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)nsv1000614
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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