A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024866



Internal ID19114083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32088082..32211780hg38UCSC Ensembl
Innerchr9:32088080..32211778hg19UCSC Ensembl
Innerchr9:32078080..32201778hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38123699
hg19123699
hg18123699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7514n100
Supporting Variantsnssv3688864
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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