A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610273



Internal ID16397682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10680430..10707753hg38UCSC Ensembl
Innerchr8:10537940..10565263hg19UCSC Ensembl
Innerchr8:10575350..10602673hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3827324
hg1927324
hg1827324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11953n54
Supporting Variantsnssv1156587
Samples1780854535_A
Known GenesC8orf74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610273
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