A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022395



Internal ID19111613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106609054..106670812hg38UCSC Ensembl
Innerchr5:105944755..106006513hg19UCSC Ensembl
Innerchr5:105972654..106034412hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3861759
hg1961759
hg1861759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746540
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)nsv1022395
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