A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009550



Internal ID19098768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109858468..110076606hg38UCSC Ensembl
Innerchr3:109577315..109795453hg19UCSC Ensembl
Innerchr3:111060005..111278143hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38218139
hg19218139
hg18218139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604407
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)nsv1009550
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