A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020027



Internal ID19109246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22740233..22778493hg38UCSC Ensembl
Innerchr9:22740232..22778492hg19UCSC Ensembl
Innerchr9:22730232..22768492hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3838261
hg1938261
hg1838261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690729
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020027
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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