A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3646996



Internal ID18945277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108293729..108341510hg38UCSC Ensembl
Innerchr5:107629430..107677211hg19UCSC Ensembl
Innerchr5:107657329..107705110hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3847782
hg1947782
hg1847782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019657
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)nssv3646996
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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