A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026827



Internal ID18769358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26693517..26904701hg38UCSC Ensembl
Innerchr9:26693515..26904699hg19UCSC Ensembl
Innerchr9:26683515..26894699hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38211185
hg19211185
hg18211185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692004
Samples
Known GenesCAAP1, PLAA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026827
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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