A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134118



Internal ID15987304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60995957..61002943hg38UCSC Ensembl
Innerchr9:39966453..39973432hg19UCSC Ensembl
Innerchr9:39956453..39963432hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386987
hg196980
hg186980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614302
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)nssv1134118
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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