A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008408



Internal ID18750939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4079539..4120843hg38UCSC Ensembl
Innerchr3:4121223..4162527hg19UCSC Ensembl
Innerchr3:4096223..4137527hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3841305
hg1941305
hg1841305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4649n100
Supporting Variantsnssv3590456, nssv3590455
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)nsv1008408
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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