A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612391



Internal ID16399800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675295..136843055hg38UCSC Ensembl
Innerchr8:137687538..137855298hg19UCSC Ensembl
Innerchr8:137756720..137924480hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38167761
hg19167761
hg18167761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122258
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612391
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