A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692002



Internal ID18990283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26453725..26670585hg38UCSC Ensembl
Innerchr9:26453723..26670583hg19UCSC Ensembl
Innerchr9:26443723..26660583hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38216861
hg19216861
hg18216861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022289
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)nssv3692002
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