A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033955



Internal ID19123177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104174067..104201402hg38UCSC Ensembl
Innerchr5:103509768..103537103hg19UCSC Ensembl
Innerchr5:103537667..103565002hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3827336
hg1927336
hg1827336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5753n100
Supporting Variantsnssv3645967
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)nsv1033955
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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