A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008061



Internal ID19097280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176282539..176317035hg38UCSC Ensembl
Innerchr3:176000327..176034823hg19UCSC Ensembl
Innerchr3:177483021..177517517hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3834497
hg1934497
hg1834497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738449
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)nsv1008061
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