A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008063



Internal ID18750594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4047125..4062494hg38UCSC Ensembl
Innerchr3:4088809..4104178hg19UCSC Ensembl
Innerchr3:4063809..4079178hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3815370
hg1915370
hg1815370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739571
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)nsv1008063
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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