A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3611346



Internal ID18909627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192016614..192044418hg38UCSC Ensembl
Innerchr3:191734403..191762207hg19UCSC Ensembl
Innerchr3:193217097..193244901hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3827805
hg1927805
hg1827805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014316
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)nssv3611346
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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