A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615077



Internal ID16402486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104834004..104834815hg38UCSC Ensembl
Innerchr9:107596285..107597096hg19UCSC Ensembl
Innerchr9:106636106..106636917hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38812
hg19812
hg18812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12829n54
Supporting Variantsnssv1140877, nssv1140879, nssv1140885, nssv1140886, nssv1140876, nssv1140884, nssv1140878, nssv1140882, nssv1140881, nssv1140880, nssv1140883
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615077
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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