A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032608



Internal ID19121830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108291492..108336206hg38UCSC Ensembl
Innerchr5:107627193..107671907hg19UCSC Ensembl
Innerchr5:107655092..107699806hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3844715
hg1944715
hg1844715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5775n100
Supporting Variantsnssv3646995
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)nsv1032608
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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