A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033890



Internal ID19123112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:119712096..119797889hg38UCSC Ensembl
Innerchr5:119047791..119133584hg19UCSC Ensembl
Innerchr5:119075690..119161483hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3885794
hg1985794
hg1885794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647976, nssv3746599
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)nsv1033890
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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