A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014472



Internal ID18757006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4092560..4124555hg38UCSC Ensembl
Innerchr3:4134244..4166239hg19UCSC Ensembl
Innerchr3:4109244..4141239hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3831996
hg1931996
hg1831996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590460
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)nsv1014472
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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