A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051901



Internal ID18794432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103009490..103037961hg38UCSC Ensembl
Innerchr9:105771772..105800243hg19UCSC Ensembl
Innerchr9:104811593..104840064hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3828472
hg1928472
hg1828472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697606
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)nsv1051901
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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