A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3606411



Internal ID18904692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161698314..161831189hg38UCSC Ensembl
Innerchr3:161416102..161548977hg19UCSC Ensembl
Innerchr3:162898796..163031671hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38132876
hg19132876
hg18132876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008088
Supporting Variants
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)nssv3606411
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