A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3612585



Internal ID18910866
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 StatusS
Merged Variantsnsv1011698
Supporting Variants
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)nssv3612585
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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