A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614697



Internal ID16402106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76533460..76545843hg38UCSC Ensembl
Innerchr9:79148376..79160759hg19UCSC Ensembl
Innerchr9:78338196..78350579hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812384
hg1912384
hg1812384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12765n54
Supporting Variantsnssv1137577
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614697
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