A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817419



Internal ID16111375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91347483..91348809hg38UCSC Ensembl
Innerchr13:91999737..92001063hg19UCSC Ensembl
Innerchr13:90797738..90799064hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381327
hg191327
hg181327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562697
Supporting Variants
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817419
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