A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614536



Internal ID18912817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164111551..164201121hg38UCSC Ensembl
Innerchr3:163829339..163918909hg19UCSC Ensembl
Innerchr3:165312033..165401603hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3889571
hg1989571
hg1889571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004324
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)nssv3614536
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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