A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647002



Internal ID18945283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108310120..108344634hg38UCSC Ensembl
Innerchr5:107645821..107680335hg19UCSC Ensembl
Innerchr5:107673720..107708234hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3834515
hg1934515
hg1834515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029462
Supporting Variants
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)nssv3647002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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