A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806043



Internal ID16099999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19205994..19235249hg38UCSC Ensembl
Innerchr13:19780134..19809389hg19UCSC Ensembl
Innerchr13:18678134..18707389hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3829256
hg1929256
hg1829256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561204
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)nssv806043
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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