A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007645



Internal ID19096864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193036916..193156958hg38UCSC Ensembl
Innerchr3:192754705..192874747hg19UCSC Ensembl
Innerchr3:194237399..194357441hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38120043
hg19120043
hg18120043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738461
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)nsv1007645
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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