A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020624



Internal ID18763159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28808326..29050315hg38UCSC Ensembl
Innerchr9:28808324..29050313hg19UCSC Ensembl
Innerchr9:28798324..29040313hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38241990
hg19241990
hg18241990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688765
Samples
Known GenesLINGO2, MIR873, MIR876
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020624
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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