A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807719



Internal ID15754989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34989272..35002484hg38UCSC Ensembl
Innerchr13:35563409..35576621hg19UCSC Ensembl
Innerchr13:34461409..34474621hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3813213
hg1913213
hg1813213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561480
Supporting Variants
Samples
Known GenesNBEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv807719
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