A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028521



Internal ID19117739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25268210..25317803hg38UCSC Ensembl
Innerchr5:25268319..25317912hg19UCSC Ensembl
Innerchr5:25304076..25353669hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3849594
hg1949594
hg1849594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745854
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)nsv1028521
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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