A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688859



Internal ID18987140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31614033..31649982hg38UCSC Ensembl
Innerchr9:31614031..31649980hg19UCSC Ensembl
Innerchr9:31604031..31639980hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3835950
hg1935950
hg1835950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021469
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)nssv3688859
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