A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036220



Internal ID18778751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102945153..103047860hg38UCSC Ensembl
Innerchr9:105707435..105810142hg19UCSC Ensembl
Innerchr9:104747256..104849963hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38102708
hg19102708
hg18102708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697599
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)nsv1036220
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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