A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005925



Internal ID19095143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3917080..3935472hg38UCSC Ensembl
Innerchr3:3958764..3977156hg19UCSC Ensembl
Innerchr3:3933764..3952156hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3818393
hg1918393
hg1818393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4639n100
Supporting Variantsnssv3590394, nssv3590395
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)nsv1005925
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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