A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007418



Internal ID19096637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68671304..68699623hg38UCSC Ensembl
Innerchr3:68720455..68748774hg19UCSC Ensembl
Innerchr3:68803145..68831464hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3828320
hg1928320
hg1828320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4772n100
Supporting Variantsnssv3594052
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)nsv1007418
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer