A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019688



Internal ID18762223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27234186..27356376hg38UCSC Ensembl
Innerchr9:27234184..27356374hg19UCSC Ensembl
Innerchr9:27224184..27346374hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38122191
hg19122191
hg18122191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692016
Samples
Known GenesEQTN, LINC00032, MOB3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019688
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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