A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117708



Internal ID15624208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88588522..89696200hg38UCSC Ensembl
Innerchr8:89600751..90708428hg19UCSC Ensembl
Innerchr8:89669867..90777550hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381107679
hg191107678
hg181107684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611713
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)nssv1117708
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