A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591199



Internal ID16378608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103403741..103493864hg38UCSC Ensembl
Innerchr3:103122585..103212708hg19UCSC Ensembl
Innerchr3:104605275..104695398hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3890124
hg1990124
hg1890124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152509
SamplesHGDP00963
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591199
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