A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014397



Internal ID18756931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:936941..1101941hg38UCSC Ensembl
Innerchr3:978625..1143625hg19UCSC Ensembl
Innerchr3:953625..1118625hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38165001
hg19165001
hg18165001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590290
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014397
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