A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035158



Internal ID19124377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55171668..55217510hg38UCSC Ensembl
Innerchr14:55638386..55684228hg19UCSC Ensembl
Innerchr14:54708139..54753981hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3845843
hg1945843
hg1845843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531025
Samples
Known GenesDLGAP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035158
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