A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688777



Internal ID18987058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29838954..29875105hg38UCSC Ensembl
Innerchr9:29838952..29875103hg19UCSC Ensembl
Innerchr9:29828952..29865103hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3836152
hg1936152
hg1836152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025884
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)nssv3688777
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