A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005014



Internal ID19094231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046103..4056386hg38UCSC Ensembl
Innerchr3:4087787..4098070hg19UCSC Ensembl
Innerchr3:4062787..4073070hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3810284
hg1910284
hg1810284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4645n100
Supporting Variantsnssv3590417
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)nsv1005014
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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