A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025828



Internal ID19115045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108299186..108340621hg38UCSC Ensembl
Innerchr5:107634887..107676322hg19UCSC Ensembl
Innerchr5:107662786..107704221hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3841436
hg1941436
hg1841436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5775n100
Supporting Variantsnssv3646997
Samples
Known GenesFBXL17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025828
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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