A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012052



Internal ID19101270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161698314..161834274hg38UCSC Ensembl
Innerchr3:161416102..161552062hg19UCSC Ensembl
Innerchr3:162898796..163034756hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38135961
hg19135961
hg18135961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4931n100
Supporting Variantsnssv3606421
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)nsv1012052
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