A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013017



Internal ID19102234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046103..4056250hg38UCSC Ensembl
Innerchr3:4087787..4097934hg19UCSC Ensembl
Innerchr3:4062787..4072934hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3810148
hg1910148
hg1810148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4645n100
Supporting Variantsnssv3739557
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)nsv1013017
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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