A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017954



Internal ID19107171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133580489..133597437hg38UCSC Ensembl
Innerchr5:132916180..132933128hg19UCSC Ensembl
Innerchr5:132944079..132961027hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3816949
hg1916949
hg1816949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648118
Samples
Known GenesFSTL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017954
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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