A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006863



Internal ID19096081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117501838..117656856hg38UCSC Ensembl
Innerchr3:117220685..117375703hg19UCSC Ensembl
Innerchr3:118703375..118858393hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38155019
hg19155019
hg18155019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3735269
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)nsv1006863
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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