A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047587



Internal ID19136806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109524667..109637699hg38UCSC Ensembl
Innerchr10:111284425..111397457hg19UCSC Ensembl
Innerchr10:111274415..111387447hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38113033
hg19113033
hg18113033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518790
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)nsv1047587
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