A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008987



Internal ID18751518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..110106hg38UCSC Ensembl
Innerchr3:60333..151789hg19UCSC Ensembl
Innerchr3:35333..126789hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3891452
hg1991457
hg1891457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590195, nssv3590194
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)nsv1008987
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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