A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028928



Internal ID18771460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20659494..20793947hg38UCSC Ensembl
Innerchr9:20659493..20793946hg19UCSC Ensembl
Innerchr9:20649493..20783946hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38134454
hg19134454
hg18134454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755833
Samples
Known GenesFOCAD, MIR491
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028928
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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