A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047506



Internal ID18790037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102880999..103104175hg38UCSC Ensembl
Innerchr9:105643281..105866457hg19UCSC Ensembl
Innerchr9:104683102..104906278hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38223177
hg19223177
hg18223177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7692n100
Supporting Variantsnssv3697597
Samples
Known GenesCYLC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047506
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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