A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014381



Internal ID18756915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158352662..158632329hg38UCSC Ensembl
Innerchr3:158070451..158350118hg19UCSC Ensembl
Innerchr3:159553145..159832812hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38279668
hg19279668
hg18279668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741554
Samples
Known GenesLOC100996447, MLF1, RSRC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014381
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer