A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1133951



Internal ID15987137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36487146..36488264hg38UCSC Ensembl
Innerchr9:36487143..36488261hg19UCSC Ensembl
Innerchr9:36477143..36478261hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614201
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)nssv1133951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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