A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140601



Internal ID15993787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102175831..102229522hg38UCSC Ensembl
Innerchr9:104938113..104991804hg19UCSC Ensembl
Innerchr9:103977934..104031625hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3853692
hg1953692
hg1853692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615021
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140601
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