A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152511



Internal ID15854166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103922314..104003499hg38UCSC Ensembl
Innerchr3:103641158..103722343hg19UCSC Ensembl
Innerchr3:105123848..105205033hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3881186
hg1981186
hg1881186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591205
Supporting Variants
Samples1780862001_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152511
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer