A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009816



Internal ID19099035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22069558..22214639hg38UCSC Ensembl
Innerchr3:22111050..22256131hg19UCSC Ensembl
Innerchr3:22086054..22231135hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38145082
hg19145082
hg18145082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589477
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)nsv1009816
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