A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014353



Internal ID19103572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108801003..108920780hg38UCSC Ensembl
Innerchr3:108519850..108639627hg19UCSC Ensembl
Innerchr3:110002540..110122317hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38119778
hg19119778
hg18119778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4834n100
Supporting Variantsnssv3735245
Samples
Known GenesGUCA1C, TRAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014353
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