A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807228



Internal ID16101184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26732521..26733725hg38UCSC Ensembl
Innerchr13:27306658..27307862hg19UCSC Ensembl
Innerchr13:26204658..26205862hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381205
hg191205
hg181205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561383
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv807228
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