A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689109



Internal ID18987390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7731398..7772496hg38UCSC Ensembl
Innerchr9:7731398..7772496hg19UCSC Ensembl
Innerchr9:7721398..7762496hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3841099
hg1941099
hg1841099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016692
Supporting Variants
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)nssv3689109
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