A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746166



Internal ID19044447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5682419..5713653hg38UCSC Ensembl
Innerchr5:5682532..5713766hg19UCSC Ensembl
Innerchr5:5735532..5766766hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3831235
hg1931235
hg1831235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028327
Supporting Variants
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)nssv3746166
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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