A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029660



Internal ID19118878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3614732..3648935hg38UCSC Ensembl
Innerchr5:3614846..3649049hg19UCSC Ensembl
Innerchr5:3667846..3702049hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3834204
hg1934204
hg1834204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746158
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029660
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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