A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614971



Internal ID16402380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101841564..101900303hg38UCSC Ensembl
Innerchr9:104603846..104662585hg19UCSC Ensembl
Innerchr9:103643667..103702406hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3858740
hg1958740
hg1858740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12813n54
Supporting Variantsnssv1140277
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614971
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