A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027435



Internal ID18769967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17068332..17095241hg38UCSC Ensembl
Innerchr5:17068441..17095350hg19UCSC Ensembl
Innerchr5:17121441..17148350hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3826910
hg1926910
hg1826910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638306
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)nsv1027435
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