A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029121



Internal ID19118340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85003541..85244596hg38UCSC Ensembl
Innerchr5:84299359..84540414hg19UCSC Ensembl
Innerchr5:84335115..84576170hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38241056
hg19241056
hg18241056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639171
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)nsv1029121
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer