A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014316



Internal ID19103537
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 StatusM
Merged Variants
Supporting Variantsnssv3611347, nssv3611346
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)nsv1014316
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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