A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615344



Internal ID16402753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127412817..127423429hg38UCSC Ensembl
Innerchr9:130175096..130185708hg19UCSC Ensembl
Innerchr9:129214917..129225529hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810613
hg1910613
hg1810613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12876n54
Supporting Variantsnssv1141452
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615344
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