A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3604387



Internal ID18902668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105114639..105344531hg38UCSC Ensembl
Innerchr3:104833483..105063375hg19UCSC Ensembl
Innerchr3:106316173..106546065hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38229893
hg19229893
hg18229893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007243
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)nssv3604387
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