A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017579



Internal ID19106796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14888888..15194226hg38UCSC Ensembl
Innerchr5:14888997..15194335hg19UCSC Ensembl
Innerchr5:14941997..15247335hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38305339
hg19305339
hg18305339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638300
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)nsv1017579
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