A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033761



Internal ID19122982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101148948..101194412hg38UCSC Ensembl
Innerchr5:100484652..100530116hg19UCSC Ensembl
Innerchr5:100512551..100558015hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3845465
hg1945465
hg1845465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645802
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)nsv1033761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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