A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614153



Internal ID16401562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33914310..34082146hg38UCSC Ensembl
Innerchr9:33914308..34082144hg19UCSC Ensembl
Innerchr9:33904308..34072144hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38167837
hg19167837
hg18167837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132845
Samples
Known GenesSNORD121A, SNORD121B, UBAP2, UBE2R2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614153
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