A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045800



Internal ID18788331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99608809..99630967hg38UCSC Ensembl
Innerchr13:100261063..100283221hg19UCSC Ensembl
Innerchr13:99059064..99081222hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3822159
hg1922159
hg1822159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525525
Samples
Known GenesCLYBL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045800
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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