A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610670



Internal ID16398079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16806085..16847396hg38UCSC Ensembl
Innerchr8:16663594..16704905hg19UCSC Ensembl
Innerchr8:16707965..16749276hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3841312
hg1941312
hg1841312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107304
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610670
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