A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029868



Internal ID19119087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..91309hg38UCSC Ensembl
Innerchr5:15520..91424hg19UCSC Ensembl
Innerchr5:68520..144424hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3875790
hg1975905
hg1875905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5513n100
Supporting Variantsnssv3636520, nssv3636519
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)nsv1029868
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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