A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034239



Internal ID18776773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:112825542..112858996hg38UCSC Ensembl
Innerchr5:112161239..112194693hg19UCSC Ensembl
Innerchr5:112189138..112222592hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3833455
hg1933455
hg1833455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647056
Samples
Known GenesAPC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034239
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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