A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746644



Internal ID19044925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:139081215..139165254hg38UCSC Ensembl
Innerchr5:138416904..138500943hg19UCSC Ensembl
Innerchr5:138444803..138528842hg18UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3884040
hg1984040
hg1884040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029030
Supporting Variants
Samples
Known GenesSIL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746644
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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