A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022712



Internal ID19111930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:92855986..93079405hg38UCSC Ensembl
Innerchr5:92191693..92415111hg19UCSC Ensembl
Innerchr5:92217449..92440867hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38223420
hg19223419
hg18223419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5716n100
Supporting Variantsnssv3639193
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)nsv1022712
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