A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029505



Internal ID19118724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28556346..28655338hg38UCSC Ensembl
Innerchr5:28556453..28655445hg19UCSC Ensembl
Innerchr5:28592210..28691202hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3898993
hg1998993
hg1898993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5612n100
Supporting Variantsnssv3635976
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)nsv1029505
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