A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025157



Internal ID19114375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120840111..120971844hg38UCSC Ensembl
Innerchr5:120175806..120307539hg19UCSC Ensembl
Innerchr5:120203705..120335438hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38131734
hg19131734
hg18131734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5801n100
Supporting Variantsnssv3647997
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)nsv1025157
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