A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615408



Internal ID16402817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128689245..128690033hg38UCSC Ensembl
Innerchr9:131451524..131452312hg19UCSC Ensembl
Innerchr9:130491345..130492133hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38789
hg19789
hg18789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1143256, nssv1143258, nssv1143257
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615408
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer