A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011698



Internal ID19100915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165541222..165580776hg38UCSC Ensembl
Innerchr3:165259010..165298564hg19UCSC Ensembl
Innerchr3:166741704..166781258hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839555
hg1939555
hg1839555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4973n100
Supporting Variantsnssv3612584, nssv3612586, nssv3612585
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)nsv1011698
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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