A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688841



Internal ID18987122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30784558..30817070hg38UCSC Ensembl
Innerchr9:30784556..30817068hg19UCSC Ensembl
Innerchr9:30774556..30807068hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3832513
hg1932513
hg1832513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026376
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)nssv3688841
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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