A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023995



Internal ID18766528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20083159..20423354hg38UCSC Ensembl
Innerchr9:20083157..20423352hg19UCSC Ensembl
Innerchr9:20073157..20413352hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38340196
hg19340196
hg18340196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755831
Samples
Known GenesMIR4473, MLLT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023995
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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