A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008169



Internal ID18750700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24337..110106hg38UCSC Ensembl
Innerchr3:66011..151789hg19UCSC Ensembl
Innerchr3:41011..126789hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3885770
hg1985779
hg1885779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590227
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)nsv1008169
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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