A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051679



Internal ID18794210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102951737..103011825hg38UCSC Ensembl
Innerchr9:105714019..105774107hg19UCSC Ensembl
Innerchr9:104753840..104813928hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3860089
hg1960089
hg1860089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697600
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)nsv1051679
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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